National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Alström Syndrome is not the name you expected.
Alström syndrome is a rare complex genetic disorder that is associated with a wide variety of symptoms affecting multiple organ systems of the body. The disorder is generally characterized by vision and hearing abnormalities, childhood obesity, insulin resistance, diabetes mellitus, heart disease (dilated cardiomyopathy) and slowly progressive kidney (renal) dysfunction, potentially leading to renal failure. The specific symptoms present and their severity may vary greatly from one person to another, even among members of the same family. Additional symptoms including lung (pulmonary), liver (hepatic) and endocrine dysfunction can also occur. Although some children may experience delays in attaining developmental milestones, intelligence is usually unaffected. Alström syndrome is caused by disruptions or defects (mutations) in the ALMS1 gene. Alström syndrome is inherited as an autosomal recessive trait.
The disorder is named after Carl-Henry Alström, a Swedish psychiatrist who, in 1959, first described the condition in the medical literature. Alström syndrome is classified as a ciliopathy, a group of disorders characterized by the defects in the function or structure of cilia. Cilia are the hair-like structures that can be found in almost all types of cells in the body.
Alström syndrome may potentially affect several different organ systems of the body. The specific symptoms associated with Alström syndrome, their severity and their rate of progression vary greatly from one person to another, even among members of the same family. It is important to note that affected individuals will not have all of the symptoms discussed below and individual cases may be dramatically different. Some symptoms may present in the first weeks of life, others symptoms may not develop until adolescence or early adulthood.
Individuals with Alström syndrome often develop vision abnormalities, specifically cone-rod dystrophy, between birth and 15 months of age. Cone-rod dystrophy is a form of retinal dysfunction. The retina is the light-sensitive membrane upon which images are focused at the back of the eye. In affected individuals, the cells in the retina (cones and rods [photoreceptors]) that convert light into nerve impulses gradually deteriorate (cone-rod dystrophy), causing vision loss. In addition to visual impairment, affected individuals may develop severe sensitivity of the eyes to light (photophobia) and rapid, involuntary eye movements (nystagmus). The progression and degree of visual impairment varies among affected individuals. Some individuals may also develop clouding of the lenses of the eyes (cataracts). In most cases, vision becomes progressively worse through the first and second decade and may result in blindness by the mid-teens. Some individual are able to read large print into their third decade.
Hearing may also be affected in Alström syndrome. Hearing is usually normal at birth, but sometime during the first decade of life, progressive sensorineural hearing loss may affect both ears (bilateral) in approximately 70% of cases. Sensorineural hearing loss is caused by an impaired ability of the auditory nerves to transmit sensory input to the brain. Hearing loss may be mild to moderate in degree or may progress to severe or moderately severe by the end of the first or second decade of life. Chronic infection or inflammation of the middle ear (otitis media) may also occur. Some individuals may develop the accumulation of thick, sticky fluid behind the eardrum (glue ear). Long-standing glue ear can cause conductive hearing loss in some cases. Conductive hearing loss is cause by the blockage of sound waves.
While vision and hearing are affected in individuals with Alström syndrome, intelligence is usually unaffected. Some infants and children may experience delays in reaching developmental milestones such as crawling or walking. Some children may have delays in developing certain language skills or develop learning disabilities.
Birth weight is normal in infants with Alström syndrome, but excessive eating beyond the normal need to satisfy hunger (hyperphagia) and rapid weight gain may occur during the first year of life. Some affected children develop childhood truncal obesity, a condition in which fat is disproportionately distributed on the abdomen and chest rather than the arms and legs. As affected individuals age, some may see their body weight fall, often regaining normal or slightly above-average weight for their size.
More than 60 percent of children with Alström syndrome develop a condition known as dilated cardiomyopathy, in which weakening of the myocardium--the heart muscle forming the walls of the heart chambers--leads to enlargement (dilatation) of the heart's lower chambers (ventricles). Dilated cardiomyopathy may not be associated with any symptoms initially, but eventually leads to weakening of the heart's pumping action, which impairs the circulation of blood through the lungs and the rest of the body resulting in fluid buildup in the heart, lung and various body tissues (congestive heart failure).
Associated symptoms and findings may depend upon the degree of heart failure, the affected child's age, and other factors. For example, in some infants, signs of heart failure may include feeding difficulties and poor weight gain, irritability, excessive sweating; labored, rapid breathing (tachypnea); bluish discoloration of the skin and mucous membranes due to abnormally low levels of circulating oxygen (cyanosis), among other findings. Children with heart failure may develop fatigue; shortness of breath (dyspnea), coughing, lack of appetite (anorexia); or abdominal pain.
The onset, severity and progression of dilated cardiomyopathy vary greatly even among members of the same family. Dilated cardiomyopathy can develop during infancy or in early adulthood. In some cases, it has preceded the development of the characteristic eye abnormalities of Alström syndrome.
Affected infants often experience insulin resistance, a condition in which the body fails to react to insulin. Insulin is a hormone secreted by the pancreas that regulates blood glucose levels by promoting the movement of glucose into cells for energy production or into the liver and fat cells for storage. Glucose is a simple sugar that is the body's primary source of energy for cell metabolism. In response to insulin resistance, the pancreas secretes more insulin, resulting in abnormally high levels of insulin in the blood (hyperinsulinemia).
Individuals with Alström syndrome eventually develop type 2 diabetes mellitus, although the age of onset varies. Children as young as five have developed type 2 diabetes mellitus. In this form of diabetes, the pancreas produces insulin but the body becomes resistant to its effects, leading to insufficient absorption of glucose and abnormally increased glucose levels in the blood (hyperglycemia) and urine. As a result, there may be a gradual onset of certain symptoms, including excessive urination (polyuria) and increased thirst (polydipsia), and the development of particular complications without appropriate treatment.
Individuals with Alström syndrome often develop a condition known as acanthosis nigricans (AN), a skin disorder characterized by abnormally increased coloration (hyperpigmentation) and "velvety" thickening (hyperkeratosis) of the skin, particularly of skin fold regions, such as of the neck and groin and under the arms (axillae). Acanthosis nigricans may be a skin manifestation of insulin resistance.
Affected individuals may also have elevated levels of certain fats (lipids) in the blood (hyperlipidemia). Hyperlipidemia is usually characterized by elevated triglycerides in the blood (hypertryglyceridemia). Some affected individuals are at risk of a rapid increase in triglycerides, which can cause inflammation of the pancreas (pancreatitis). Pancreatitis can be associated with abdominal pain, chills, jaundice, weakness, sweating, vomiting, and weight loss.
Some males with Alström syndrome may experience diminished hormone production by the testes (hypogonadotrophic hypogonadism). The onset of puberty may be delayed. Some affected males may develop abnormally enlarged breasts (gynecomastia).
Hypogonadism also occurs in affected females, but may not be apparent until puberty. Affected females may develop polycystic ovarian syndrome (PCOS). PCOS can result in irregular menstrual periods or a lack of menstruation, oily skin that is prone to acne, cysts on the ovaries and mild hirsutism (a male pattern of hair growth). Hair may develop on the upper lip and chin. PCOS may occur as a symptom of insulin resistance. In some cases, females enter puberty early (before the age of 8), a condition called precocious puberty.
Some individuals with Alström syndrome develop various urological abnormalities. As with other symptoms, the severity of urological abnormalities can vary greatly. Affected individuals may be unable to coordinate the muscles of the bladder and the tube that carries urine from the bladder out of the body (urethral dyssynergia). Additional abnormalities include difficulty beginning urination, reduced flow, increased time between urinating, inability to control bowel and bladder movements (incontinence), and urinary retention. Urinary abnormalities may alternate between underactivity and overactivity of the bladder. Many individuals with Alström syndrome also have recurrent urinary tract infections.
Affected individuals often experience slowly progressive dysfunction of the kidneys. Onset of kidney dysfunction may be during childhood or adulthood. In many cases, early kidney dysfunction may not cause symptoms (asymptomatic). Two common signs of kidney disease are excessive urination (polyuria) and excessive thirst (polydipsia). Eventually, symptoms including swelling of the ankles or a general feeling of ill health (malaise) may develop. Kidney dysfunction may progressively worsen eventually causing end stage renal failure, which can occur as early as the mid or late teen-aged years.
Some individuals may develop breathing (respiratory) or lung (pulmonary) problems such as chronic respiratory infections beginning early during childhood. These chronic infections can contribute to the development of asthma, chronic inflammation of the sinuses (sinusitis), a dry cough, and repeated episodes of inflammation of the bronchial tubes (bronchitis) or pneumonia. More serious pulmonary complications can occur including high blood pressure of the main artery of the lungs (pulmonary hypertension), chronic obstructive pulmonary disease (COPD), acute respiratory distress syndrome, and emphysema.
The liver may be involved in some cases resulting in abnormal enlargement of the liver (hepatomegaly). The severity of liver involvement can range from elevated liver enzymes, which are common in childhood to fatty liver disease (steatohepatitis). Steatohepatitis is characterized by the accumulation of fatty material in the liver and is often associated with diabetes or obesity. Liver (hepatic) dysfunction may occur and can progress to cause scarring (cirrhosis) within the liver, high blood pressure of the main vein of the liver (portal hypertension), abnormal enlargement of the spleen (splenomegaly), the abnormal accumulation of fluid in the abdominal cavity (ascites) and, eventually, liver failure by the second or third decade.
Additional serious complications associated with liver disease including esophageal varices and hepatic encephalopathy can develop. Esophageal varices are damaged, swollen blood vessels in the throat that are prone to bleeding and can rupture potentially causing life-threatening bleeding complications. Hepatic encephalopathy is a brain disorder that occurs in some individuals with chronic liver disease. It is a complex disorder that encompasses a spectrum of disease ranging from a subtle condition with no outward signs to a severe form that can cause life-threatening neurological complications.
Additional symptoms may be associated with Alström syndrome including low levels of growth hormone, which may result in short stature in adulthood; high blood pressure (hypertension), abnormally decreased activity of the thyroid gland and underproduction of thyroid hormones (hypothyroidism), advanced bone age; patchy areas of hair loss (alopecia); gastroesophageal reflux; pain in the middle of the abdomen just below the sternum (epigastric pain); and abnormal side-to-side (scoliosis) or front-to-back (kyphosis) curvature of the spine.
A variety of neurobehavioral findings have been reported including seizures, decreased reflexes (hyporeflexia), exaggerated response when startled, unexplained joint or muscle pain and dystonia, a group of neurological conditions generally characterized by involuntary muscle contractions that force the body into abnormal, sometimes painful movements and positions.
Alström syndrome is caused by mutations in the ALMS1 gene. Genes provide instructions for creating proteins that play a critical role in many functions of the body. When a mutation of a gene occurs, the protein product may be faulty, inefficient, or absent. Depending upon the functions of the particular protein, this can affect many organ systems of the body, including the brain.
In Alström syndrome, the gene mutation is inherited as an autosomal recessive trait. Genetic diseases are determined by the combination of genes for a particular trait that are on the chromosomes received from the father and the mother.
Recessive genetic disorders occur when an individual inherits the same abnormal gene for the same trait from each parent. If an individual receives one normal gene and one gene for the disease, the person will be a carrier for the disease, but usually will not show symptoms. The risk for two carrier parents to both pass the defective gene and, therefore, have an affected child is 25% with each pregnancy. The risk to have a child who is a carrier like the parents is 50% with each pregnancy. The chance for a child to receive normal genes from both parents and be genetically normal for that particular trait is 25%. The risk is the same for males and females. Consanguinity increases the probability that parents convey the disease to the offspring.
Investigators have determined that theALMS1 gene is located on the short arm (p) of chromosome 2 (2p13). Chromosomes, which are present in the nucleus of human cells, carry the genetic information for each individual. Human body cells normally have 46 chromosomes. Pairs of human chromosomes are numbered from 1 through 22 and the sex chromosomes are designated X and Y. Males have one X and one Y chromosome and females have two X chromosomes. Each chromosome has a short arm designated "p" and a long arm designated "q". Chromosomes are further sub-divided into many bands that are numbered. For example, "chromosome 2q13" refers to band 13 on the long arm of chromosome 2. The numbered bands specify the location of the thousands of genes that are present on each chromosome.
The ALMS1 gene contains instructions for creating (encoding) a specific protein known as ALMS1. The role and function of this protein in the body is not fully understood, but believed to be involved in ciliary function, cell cycle control and intracellular transport. The ALMS1 protein is expressed in all organ tissues of the body (ubiquitously expressed). Research is underway to determine this protein's exact functions, which should greatly increase the understanding of Alström syndrome. Because symptoms of Alström syndrome vary greatly among family members, researchers suspect that additional genetic or environmental factors may play a role in the development and progression of Alström syndrome.
As mentioned above, some research has indicated that the protein encoded by the ALMS1 gene has a role in the proper function, formation, and/or maintenance of cilia, the hair-like structures that can be found in almost all types of cells in the body, and possibly some related structures such as the basal body (which "anchors" the cilia to a cell). A related disorder known as Bardet-Biedl syndrome has also been linked to ciliary dysfunction. Several disorders, referred to as ciliopathies, have been linked to ciliary dysfunction. More research is necessary to determine what role, if any, that cilia and related structures play in the development of Alström syndrome.
Alström syndrome affects males and females in equal numbers. The exact incidence is unknown. Estimates have ranged from 1 in 10,000 to fewer than 1 in 1,000,000 individuals in the general population. Approximately 800 cases have been identified worldwide. Because some cases of Alström syndrome may go unrecognized or misdiagnosed, the disorder may be under-diagnosed, making it difficult to determine its true frequency in the general population.
Alström syndrome occurs with greater frequency in ethnically isolated communities such as French Acadians and Pakistanis.
Symptoms of the following disorders can be similar to those of Alström syndrome. Comparisons may be useful for a differential diagnosis.
Bardet-Biedl syndrome is a rare, genetic multisystem disorder characterized primarily by deterioration of the cells that receive light stimuli (rod and cone cells) in the retina of the eyes (progressive rod-cone dystrophy), an extra finger near the pinky or an extra toe near the fifth toe (postaxial polydactyly), a condition in which fat is disproportionately distributed on the abdomen and chest rather than the arms and legs (truncal obesity), diminished size and decreased function of the gonads (testes) in males (hypogonadism), kidney (renal) abnormalities, and learning difficulties. Visual abnormalities usually become progressively worse and may ultimately result in blindness. Kidney (renal) abnormalities may progress to cause life-threatening complications. Learning difficulties are a common finding due, in part, to vision loss. Only a minority of affected individuals have severe mental impairment. Most cases of Bardet-Biedl syndrome are inherited as an autosomal recessive trait. Bardet-Biedl syndrome shows significant overlap with a disorder called Laurence-Moon syndrome. In fact, in the past, these disorders were considered the same and referred to as Laurence-Bardet-Biedl syndrome. Eventually, researchers decided that the two disorders despite numerous similarities were distinct entities. However, recent research has demonstrated that some individuals with the clinical findings of Laurence-Moon syndrome have had mutations in genes linked to Bardet-Biedl syndrome. This discovery has led some researchers to suggest that little evidence exists to continue to classify these two disorders as distinct entities. (For more information on these disorders, choose "Bardet-Biedl" or "Laurence-Moon" as your search term in the Rare Disease Database.)
Leber congenital amaurosis (LCA) is a rare genetic eye disorder. Affected infants are often blind at birth or loss their sight within the first few of years of life. Other symptoms may include crossed eyes (strabismus); rapid, involuntary eye movements (nystagmus); unusual sensitivity to light (photophobia); clouding of the lenses of the eyes (cataracts); and/or abnormal protrusion of the front (anterior), clear portion of the eye through which light passes (cornea) (keratoconus). In addition, some infants may exhibit hearing loss, intellectual disability, and/or a delay in the acquisition of skills that require the coordination of mental and muscular activity (psychomotor retardation). Leber congenital amaurosis is inherited as an autosomal recessive trait. (For more information on this disorder, choose "Leber Congenital Amaurosis" as your search term in the Rare Disease Database.)
Usher syndrome is a rare genetic disorder primarily characterized by deafness due to an impaired ability of the auditory nerves to transmit sensory input to the brain (sensorineural hearing loss) accompanied by retinitis pigmentosa, a disorder that causes progressive loss of vision. Researchers have identified three types of Usher's syndrome and debated the existence of a fourth type. The age at which the disorder appears along with the severity of symptoms distinguishes the different types of Usher syndrome. Usher syndrome may be associated with failure of muscle coordination (ataxia) and night blindness. Usher syndrome is inherited as an autosomal recessive trait. The possible fourth type of Usher syndrome may be inherited as an X-linked trait. (For more information on this disorder, choose "Usher" as your search term in the Rare Disease Database.)
Mitochondrial disorders are a group of inherited disorders characterized by mutations affecting the parts of the cell that release energy (mitochondria). Mitochondrial diseases often hamper the ability of affected cells to break down food and oxygen and produce energy. In most mitochondrial disorders, abnormally high numbers of defective mitochondria are present in the cells of the body. Mitochondrial diseases often affect more than one organ system of the body and can be associated with similar symptoms to Alström syndrome including cardiomyopathy, sensorineural hearing loss, vision abnormalities and diabetes mellitus. Mitochondrial disorders that share similar characteristics to Alström syndrome include Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia (CPEO). (For more information, choose the specific disorder name as your search term in the Rare Disease Database.)
A diagnosis of Alström syndrome is made upon a thorough clinical evaluation, identification of characteristic findings (e.g., cone-rod dystrophy, sensorineural hearing impairment, cardiomyopathy, obesity, kidney dysfunction, diabetes), and a variety of specialized tests. A diagnosis of Alström syndrome may be difficult because of delayed onset of certain key characteristics including diabetes, cardiomyopathy, and kidney disease. The absence of certain findings (e.g., polydactyly, intellectual disability) distinguishes Alström syndrome from similar syndromes such as Bardet-Biedl syndrome or Laurence-Moon syndrome.
Clinical Testing and Work-Up
An eye specialist (ophthalmologist) using specialized tests can make diagnosis of disorders affecting the retina of the eye such as Alström syndrome. An electroretinogram (ERG) may be used to detect abnormalities in the retina, and an electro-oculogram (EOG) may be used to measure retinal function. Sensorineural deafness may be confirmed through a variety of specialized hearing (auditory) tests.
Individuals with a suspected diagnosis of Alström syndrome should receive a thorough physical examination to detect the potential presence of additional heart, endocrinological, and kidney abnormalities often associated with Alström syndrome.
Molecular genetic testing can confirm a diagnosis of Alström syndrome. Molecular genetic testing can detect mutations in the ALMS1 gene known to cause the disorder, but is available only on a clinical basis. Molecular genetic testing detects ALMS1 mutations in approximately 70%-80% of individuals of Northern European descent and in approximately 40% of individuals worldwide.
There is no specific treatment for individuals with Alström syndrome. Treatment is directed toward the specific symptoms that are apparent in each individual. Treatment may require the coordinated efforts of a team of specialists. Pediatricians, surgeons, cardiologists, specialists who asses and treat hearing problems (audiologists), specialists who asses and treat vision problems (ophthalmologists), specialists who deal with the system of glands that secrete hormones into the bloodstream (endocrinologists), specialists who assess and treat skeletal problems (orthopedists), and other healthcare professionals may need to systematically and comprehensively plan an affect child's treatment.
Photophobia may be treated with specially-tinted, prescription glasses. In cases where cataracts significantly interfere with vision, they may be removed surgically. Whether or not surgery helps to improve vision often depends on how far the retinal changes have advanced.
Various vision aids may help people with Alström syndrome to make the maximum use of their remaining vision. These include optical aids such as Corning and NOIR glasses, the Fresnel Prising telescope, microscopes, and night vision devices. Non-optical aids that may also be useful include the Apollo Laser, Visualtek closed circuit television, the Wide Angle Mobility Light, paper guides, large-print typewriters, and adjustable stands. There are also reading machines and talking computers that can enhance the quality of life for individuals whose vision is severely impaired by Alström syndrome.
Children with Alström syndrome should receive instruction while they retain sight. Physicians have recommended that children learn mobility training, adaptive living skills, computing skills such as voice recognition and transcription software, and the use of Braille before sight is lost.
There is no specific treatment for sensorineural hearing loss. Hearing aids may help to maximize remaining hearing, and speech therapy may enhance the ability of a child to communicate orally. In the case of deafness associated with Alström syndrome, teaching a child sign language may not be an option as vision loss may also occur. Therefore, educational methods and options should be chosen carefully. A surgical procedure called a myringotomy, in which a thin incision is made in the eardrum to release fluid, may be performed for individuals with glue ear. Cochlear implants, which improve hearing by stimulating nerve fibers within the inner ear, have been beneficial in some cases. Tactile language could be of help for some deaf-blind individuals.
Strict dietary measures and exercise programs may help to control obesity, as well as aid in the management of diabetes mellitus and/or glucose intolerance associated with Alström syndrome. In most of the diagnosed cases of Alström syndrome, diabetes was controlled by diet and exercise alone. However, it was necessary in some cases to treat the diabetes with oral anti-diabetic agents or insulin. Patients may control diabetes for many years with insulin-sensitizing agents such as metformin. In several individuals, the group of incretins agents such as the Glucagon-like peptide 1 (GLP-1) analogues and the dipeptidyl peptidase-4 (DPP-4) inhibitors have been used with success.
If insulin therapy should become necessary for diabetes associated with Alström syndrome, a daily routine of insulin-injection, a controlled diet, exercise to burn off glucose, and testing for blood sugar level is vital in achieving and maintaining good blood sugar control. Self-monitoring of blood glucose levels uses a single drop of blood which is obtained with a finger stick, and placed on a chemically treated pad on a plastic strip; the color change of the chemically treated pad is compared to a color chart or "read" by a battery-operated portable meter.
Insulin must be given by injection, usually two or more times each day. Portable "insulin pumps" have been developed that permit continuous administration of insulin, as well as additional amounts of insulin when needed to control the changes in blood sugar level that occur after meals.
The management of diabetes may reduce the risk of kidney failure. If excess levels of protein are detected in the urine (proteinuria), drugs known as angiotensinogen-converting enzyme (ACE) inhibitors may be recommended. In the event of kidney failure a procedure to remove toxins from the blood (dialysis) may be necessary. Kidney transplantation has been successfully performed in a growing number of individuals with Alström syndrome. However, the procedure can be contraindicated by other potential complications of the disorder such as morbid obesity, uncontrolled diabetes or cardiomyopathy.
Hypertriglyceridemia may be treated with a low-fat diet or lipid lowering medications.
Cardiac abnormalities may be treated with a variety of drugs including ACE inhibitors, which relax blood vessels, thereby lowering the blood pressure and minimizing the effort needed by the heart to pump blood throughout the body; drugs that reduce abnormal fluid retention by promoting the production and excretion of water and sodium from the body through the urine (diuretics); drugs such as digoxin that increase the efficiency of heart muscle contractions and produce a more regular heartbeat; and, in some cases, drugs that reduce the workload of the heart by blocking certain substances from binding to structures within the heart (beta blockers). In rare, isolated cases, a heart (cardiac) transplant has been successfully performed on individuals with Alström syndrome.
As children attain puberty, an evaluation should be performed to see whether hormonal adjustment therapy is necessary. For example, male hypogonadism should be treated with testosterone to preserve sexuality, muscle strength and bone health. Individuals who have hypothyroidism may be treated with L-thyroxine, a type of thyroid hormone. Pediatric patients may be treated with recombinant growth hormone to promote their linear growth. In adult patients growth hormone therapy may benefit body composition (the balance between the fat mass and fat free mass) and bone health. Some female disorders such as irregular menses, PCOS and hyperandrogenism may be treated with estrogen and progestin. Female individuals with PCOS and who are overweight and have diabetes may benefit from treatment with diet, exercise and insulin-sensitizing agents such as metformin.
A variety of techniques may be used to treat the complications of liver involvement. Portal hypertension may be treated with beta-blocker drugs. Sclerotherapy may be used to treat esophageal varices. Sclerotherapy is a procedure in which a solution, called a sclerosant or sclerosing agent, is injected directly into the affected veins of the throat and the areas adjacent to the affected veins. The solution injected into the veins causes blood clots to form in the veins stopping bleeding. The solution injected into the surrounding areas causes stops bleeding by thickening and swelling the vein to compress the blood vessel.
Banding (the application of rubber bands at the bleeding site) may be done to prevent bleeding in the upper gastrointestinal tract. Individuals who fail to respond to other methods may be candidates for transjugular intrahepatic portosystemic shunt (TIPS). During this procedure, a small metal device called a stent is placed into the liver creating an artificial passage from the portal vein to the hepatic vein, thereby improving blood flow. It can decrease the risk of variceal bleeding associated with portal hypertension. Some individuals with severe liver complications may be evaluated for a liver transplantation.
Genetic counseling may be of benefit for affected individuals and their families. Other treatment is symptomatic and supportive.
Researchers at the Jackson Laboratory in Bar Harbor, Maine maintain a registry for Alström syndrome that contains an ongoing database of patients in more than 50 different countries.
Alstrom Syndrome Registry
Phone: 207.288.6385; 800.371.3628
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Toll-free: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Marshall JD. Alstrom Syndrome. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:305-06.
Marshall JD, Maffei P, Beck S, et al. Clinical utility gene car for: Alstrom syndrome – updated 2013.Eur J Human Genet.2013;61:[Epub ahead of print]. //www.ncbi.nlm.nih.gov/pubmed/23612576
Collin GB, Marshall JD, King BL, et al. The Alstrom syndrome protein, ALMS1, interacts with a-actinin and components of the endosome recycling pathway. PLoS One. 2012;7:e37925. //www.ncbi.nlm.nih.gov/pmc/articles/PMC3365098/
Marshall JD, Maffei P, Collin GB, Naggert JK. Alstrom syndrome: genetics and clinical overview. Curr Genomics. 2011;12:225-235. //www.ncbi.nlm.nih.gov/pubmed/22043170
Jagger D, Collin G, Kelly J, et al. Alstrom syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity. Hum Mol Genet. 2011;20:466-481. //www.ncbi.nlm.nih.gov/pubmed/21071598
Joy T, Cao H, Black G, et al. Alstrom syndrome (OMIM 203800): a case report and literature review. Orphanet J Rare Dis. 2007;2:49. //www.ncbi.nlm.nih.gov/pmc/articles/PMC2266715/
Marshall JD, Hinman EG, Collin GB, et al. Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alstrom syndrome. Hum Mutat. 2007;28:1114-11123.//www.ncbi.nlm.nih.gov/pubmed/17594715
Minton JAL, Owen KR, Ricketts CJ, et al. Syndromic obesity and diabetes: changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alstrom syndrome. J Clin Endocrinol Metab. 2006;91:3110-6.//www.ncbi.nlm.nih.gov/pubmed/16720663
Badaon JL, Mtisuma N, Beales PL, Katsanis N. The ciliopathies: an emerging class of human genetic disorders. Ann Rev Genomics Human Genet. 2006;22:125-48.//www.ncbi.nlm.nih.gov/pubmed/16722803
Marshall JD, Bronson RT, Collins GB, et al. New Alstrom syndrome phenotypes based on evaluation of 182 cases. Arch Intern Med. 2005;165:675-83.//www.ncbi.nlm.nih.gov/pubmed/15795345
Hearn T, Spalluto C, Phillips VJ, et al. Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance and type 2 diabetes. Diabetes. 2005;54:1581-7.//www.ncbi.nlm.nih.gov/pubmed/15855349
Makaryus AN, Popkowski B, Kort S, Paris Y, Mangion J. A rare case of Alstrom syndrome presenting with rapidly progressive severe dilated cardiomyopathy diagnosed by echocardiography. J Am Soc Echocardiogr. 2003;16:194-96.//www.ncbi.nlm.nih.gov/pubmed/12574750
Maffei P, Boschetti M, Marshall JD, et al. The Alstrom syndrome: is it a rare or unknown disease? Ann Ital Med Int. 2002;17:221-28.//www.ncbi.nlm.nih.gov/pubmed/12532560
Collin GB, Marshall JD, Boerkoel CF, et al. Alstrom syndrome: further evidence for linkage to human chromosome 2p13. Hum Genet. 1999;105:474-79.//www.ncbi.nlm.nih.gov/pubmed/10598815
Russell-Eggitt IM, Clayton PT, Coffey R, et al. Alstrom syndrome. Report of 22 cases and literature review. Ophthalmology. 1998;105:1274-80.//www.ncbi.nlm.nih.gov/pubmed/9663233
Marshall JD, Ludman MD, Shea SE, et al. Genealogy, natural history, and phenotype of Alstrom syndrome in a large Acadian kindred and three additional families. Am J Med Genet. 1997;73:150-61.//www.ncbi.nlm.nih.gov/pubmed/9409865
Collin GB, Marshall JD, Cardon LR, et al. Homozygosity mapping Alstrom syndrome to chromosome 2p. Hum Mol Genet. 1997;6:213-19.//www.ncbi.nlm.nih.gov/pubmed/9063741
Tremblay F, LaRoche RG, Shea SE, et al. Longitudinal study of the early electroretinographic changes in Alstrom's syndrome. Am J Ophthalmol. 1993;115:657-65.//www.ncbi.nlm.nih.gov/pubmed/8488920
Marshall JD, Paisey RB, Carey C, Macdermott S. Alstrom Syndrome. 2003 Feb 7 [Updated 2012 May 31]. In: Pagon RA, Bird TD, Dolan CR, et al.,GeneReviews. Internet. Seattle, WA: University of Washington, Seattle; 1993-. Available at://www.ncbi.nlm.nih.gov/books/NBK1267/
McKusick VA., ed. Online Mendelian Inheritance in Man (OMIM). Baltimore. MD: The Johns Hopkins University; Entry No:203800; Last Update:10/02/2012. Available at: //omim.org/entry/203800 Accessed on: June 10, 2013.
Alström Syndrome International
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Alström Syndrome UK
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American Academy of Audiology
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American Society for Deaf Children
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Better Hearing Institute
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Blind Children's Center
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- Email: email@example.com
- Website: //www.blindchildrenscenter.org
- Chiltern Court, Unit 10
- Asheridge Rd Ind
- Chesham, HP5 2PX
- United Kingdom
- Tel: 4401494791224
- Fax: 4401494797199
- Tel: 8000181024
- Email: firstname.lastname@example.org
- Website: //www.cardiomyopathy.org
Children's Cardiomyopathy Foundation
- PO Box 547
- Tenafly, NJ 7670
- Tel: (866)808-2873
- Fax: (201)227-7016
- Email: email@example.com
- Website: //www.childrenscardiomyopathy.org
Foundation Fighting Blindness
- 7168 Columbia Gateway Drive, Suite 100
- Columbia, MD 21046
- Tel: (410)423-0600
- Fax: (410)872-0574
- Tel: (800)683-5555
- Email: info@FightBlindness.org
- Website: //www.blindness.org/
Genetic and Rare Diseases (GARD) Information Center
- PO Box 8126
- Gaithersburg, MD 20898-8126
- Tel: (301)251-4925
- Fax: (301)251-4911
- Tel: (888)205-2311
- Website: //rarediseases.info.nih.gov/GARD/
Little People of America, Inc.
- 250 El Camino Real Suite 201
- Tustin, CA 92780
- Tel: (714)368-3689
- Fax: (714)368-3367
- Tel: (888)572-2001
- Email: firstname.lastname@example.org
- Website: //www.lpaonline.org/
March of Dimes
- 1275 Mamaroneck Avenue
- White Plains, NY 10605
- Tel: (914)997-4488
- Fax: (914)997-4763
- Email: AskUs@marchofdimes.org or email@example.com
- Website: //www.marchofdimes.org and nacersano.org
NIH/National Eye Institute
- 31 Center Dr
- MSC 2510
- Bethesda, MD 20892-2510
- United States
- Tel: (301)496-5248
- Fax: (301)402-1065
- Email: firstname.lastname@example.org
- Website: //www.nei.nih.gov/
NIH/National Institute on Deafness and Other Communication Disorders
- 31 Center Drive, MSC 2320
- Communication Avenue
- Bethesda, MD 20892-3456
- Tel: (301)402-0900
- Fax: (301)907-8830
- Tel: (800)241-1044
- Email: email@example.com
- Website: //www.nidcd.nih.gov
National Association for Parents of Children with Visual Impairments (NAPVI)
- P.O. Box 317
- Watertown, MA 02272-0317
- Tel: (617)972-7441
- Fax: (617)972-7444
- Tel: (800)562-6265
- Email: firstname.lastname@example.org
- Website: //www.napvi.org
National Consortium on Deaf-Blindness
- The Teaching Research Institute
- 345 N. Monmouth Avenue
- Monmouth, OR 97361
- Tel: (800)438-9376
- Fax: (503)838-8150
- Tel: (800)438-9376
- Email: email@example.com
- Website: //www.nationaldb.org
Perkins School for the Blind
- 175 North Beacon Street
- Watertown, MA 2472
- Tel: (617)924-3434
- Fax: (617)926-2027
- Email: Info@Perkins.org
- Website: //www.Perkins.org
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.
For additional information and assistance about rare disorders, please visit the National Organization for Rare Disorders web site at www.rarediseases.org
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
Last Updated: 6/29/2015
Copyright 2013 National Organization for Rare Disorders, Inc.
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