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Results 11 - 20 of 1,007 for Brain disorder
  1. GABA-transaminase deficiency 
    GABA-transaminase deficiency is a brain disease (encephalopathy) that begins in infancy. Babies with this disorder have recurrent seizures (epilepsy), uncontrolled limb movements (choreoathetosis), exaggerated reflexes (hyperreflexia), weak ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  2. MECP2 gene 
    ... been identified in females with Rett syndrome, a brain disorder that causes problems with communication, learning, and coordination. ... ML, LaSalle JM. The role of MeCP2 in brain development and neurodevelopmental disorders. Curr Psychiatry Rep. 2010 Apr;12(2):127- ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  3. Perry syndrome 
    Perry syndrome is a progressive brain disease that is characterized by four major features: a pattern of movement abnormalities known as parkinsonism, psychiatric changes, weight loss, and abnormally ...
    https://medlineplus.gov/genetics/condition/perry-syndrome - Genetics
  4. DCTN1 gene 
    ... one DCTN1 gene mutation is associated with a brain disorder called frontotemporal dementia (FTD) without the features of ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  5. Acute necrotizing encephalopathy type 1 
    ... 3 or IIAE3, is a rare type of brain disease (encephalopathy) that occurs following a viral infection such ... Zhang HL. Acute necrotizing encephalopathy: an underrecognized clinicoradiologic disorder. ... or Free article on PubMed Central
    https://medlineplus.gov/.../acute-necrotizing-encephalopathy-type-1 - Genetics
  6. VRK1 gene 
    ... VRK1 gene are thought to cause another rare brain disorder that has been described as a form of ... sensory neuropathy (HMSN). HMSNs are a group of disorders that affect peripheral nerves, which connect the brain and spinal cord to muscles as well as ...
    https://medlineplus.gov/genetics/gene/vrk1 - Genetics
  7. MAPT gene 
    ... gene have also been found to cause other brain disorders similar to FTDP-17 and progressive supranuclear palsy. ... on cell function and survival is unknown, these disorders are characterized by the death of brain cells in regions of the brain essential for ...
    https://medlineplus.gov/genetics/gene/mapt - Genetics
  8. COQ2 gene 
    ... the risk of multiple system atrophy, a progressive brain disorder that affects movement and balance and disrupts the ... many parts of the body, most often the brain, muscles, and kidneys. The COQ2 gene mutations associated with this disorder greatly reduce or eliminate the production of the ...
    https://medlineplus.gov/genetics/gene/coq2 - Genetics
  9. MTOR gene 
    ... Dobyns WB. Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism. ...
    https://medlineplus.gov/genetics/gene/mtor - Genetics
  10. Depression 
    ... disorder occurs together with features of schizophrenia (a brain disorder that affects a person's thinking, sense of ... associated with depression have diverse functions in the brain. Some of these ... The disorder can be triggered by substance abuse, certain medications, ...
    https://medlineplus.gov/genetics/condition/depression - Genetics
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