Aniridia Cerebellar Ataxia Mental Deficiency
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Aniridia Cerebellar Ataxia Mental Deficiency is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Aniridia-Cerebellar Ataxia-Mental Retardation
- Aniridia, Partial-Cerebellar Ataxia-Mental Retardation
- Aniridia, Partial-Cerebellar Ataxia-Oligophrenia
- Gillespie Syndrome
Aniridia, cerebellar ataxia, and mental deficiency, also known as Gillespie syndrome, is an extremely rare inherited disorder that is characterized by the absence, in whole (aniridia) or in part (partial aniridia), of the colored portion (iris) of the eye; impaired coordination of voluntary movements due to underdevelopment (hypoplasia) of the brain's cerebellum (cerebellar ataxia); and mental retardation. The condition usually affects both eyes (bilateral) but a few cases have been reported in which only one eye is affected. Some individuals with this syndrome also exhibit a delay in the acquisition of skills requiring coordination of muscular and mental activity (psychomotor retardation). ACAMD is thought to be inherited as an autosomal recessive genetic trait and is extremely rare, with only 20 to 30 cases reported in the medical literature.
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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
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Last Updated: 1/5/1970
Copyright 2007 National Organization for Rare Disorders, Inc.
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