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Results 1 - 10 of 20 for Intellectual "disability," progressive
  1. ... Wevers RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am J Hum ...
  2. ... paraplegia type 15. This condition is characterized by progressive movement problems, intellectual disability, and vision problems. Many of the ZFYVE26 gene ...
  3. ... brain abnormalities associated with this condition lead to intellectual disability, weak muscle tone (hypotonia), and progressive muscle stiffness (spasticity) in affected individuals. Brain malformations ...
  4. ... identified in people with infantile neuroaxonal dystrophy, a progressive neurological disorder that causes intellectual disability and movement problems. Mutations in the PLA2G6 gene ...
  5. ... is characterized by abnormal brain function (encephalopathy) and ... progressive encephalopathy with or without lipodystrophy typically do not ...
  6. ... lenses of the eyes (cataracts), developmental delay, or intellectual ... lead to the progressive movement problems of SPG9A and SPG9B; however, the ...
  7. ... causes MECP2 duplication syndrome, a condition characterized by intellectual disability, delayed development, and seizures. This condition affects males ...
  8. ... consequently, the nervous system, causing severe learning problems, intellectual disability, and the other features of fragile X syndrome. ... have learning disabilities, attention-deficit/hyperactivity disorder (ADHD), ... or developmental disorders that affect communication and social ...
  9. ... features of the condition, such as slow growth, intellectual disability, and brittle hair, likely result from problems with ... cancer, short stature, hearing loss, poor coordination, and intellectual disability.Researchers are uncertain how variants in this single ...
  10. ... an unusually large head size (macrocephaly), tall stature, intellectual disability, seizures, ataxia, and other health problems. Researchers are ... encephalopathy caused by CACNA1A gene variants often experience intellectual disability, ataxia, nystagmus, and weak muscle tone (hypotonia). Studies ...
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