Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 51 - 60 of 1,007 for Brain disorder
  1. Developmental and epileptic encephalopathy 1 
    ... spasms can also have nongenetic causes, such as brain malformations, other disorders that affect brain function, or brain damage. In addition, changes in ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  2. Adenylosuccinate lyase deficiency 
    Adenylosuccinate lyase deficiency is a neurological disorder that causes brain dysfunction (encephalopathy) leading to delayed development of mental and movement abilities (psychomotor delay), autistic characteristics that affect communication and social interaction, and ...
    https://medlineplus.gov/.../adenylosuccinate-lyase-deficiency - Genetics
  3. X-linked creatine deficiency 
    ... is an inherited disorder that primarily affects the brain. People with this disorder have intellectual disability, which can range from mild to severe, and delayed speech development. Some affected individuals develop behavioral ...
    https://medlineplus.gov/.../condition/x-linked-creatine-deficiency - Genetics
  4. Arginine:glycine amidinotransferase deficiency 
    ... is an inherited disorder that primarily affects the brain. People with this disorder have mild to moderate intellectual disability and delayed speech development. Some affected individuals develop autistic behaviors that affect communication ...
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency - Genetics
  5. Primary familial brain calcification 
    ... The main signs and symptoms of primary familial brain calcification are movement disorders and psychiatric or behavioral problems. These difficulties usually ...
    https://medlineplus.gov/.../primary-familial-brain-calcification - Genetics
  6. RNAse T2-deficient leukoencephalopathy 
    ... and the ventricles. An abnormally small head and brain size (microcephaly) often occurs in this disorder. The prevalence of RNAse T2-deficient leukoencephalopathy is ...
    https://medlineplus.gov/.../rnase-t2-deficient-leukoencephalopathy - Genetics
  7. Autosomal dominant nocturnal frontal lobe epilepsy 
    ... dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder. Brain. 1995 Feb;118 ( Pt 1):61-73. doi: ...
    https://medlineplus.gov/...-dominant-nocturnal-frontal-lobe-epilepsy - Genetics
  8. CUL3-related neurodevelopmental disorder 
    ... mutation in a Japanese patient with autism spectrum disorder. Brain Dev. 2021 Feb;43(2):303-307. doi: ... CUL3 variant in a patient with neurodevelopmental delay. Brain Dev. 2023 Apr;45(4):244-249. doi: 10.1016/j.braindev.2023.01.003. Epub 2023 Jan 27. Citation on PubMed
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  9. CDKL5 gene 
    ... CDKL5 and MeCP2 proteins may interact in the brain, the two disorders might be caused by a similar mechanism.Mutations ... of CDKL5 or impairment of its function disrupts brain development, but it is ... disorder.Most CDKL5 gene mutations change single protein building ...
    https://medlineplus.gov/genetics/gene/cdkl5 - Genetics
  10. MECP2-related severe neonatal encephalopathy 
    ... ML, LaSalle JM. The role of MeCP2 in brain development and neurodevelopmental disorders. Curr Psychiatry Rep. 2010 Apr;12(2):127- ...
    https://medlineplus.gov/...p2-related-severe-neonatal-encephalopathy - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next