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 11 - 20 of 363 for Brain disorder
  1. ATN1 gene 
    ... 35. Dentatorubral-pallidoluysian atrophy (DRPLA) is a progressive brain disorder that causes involuntary movements, mental and emotional problems, ... features, and skeletal abnormalities. Many affected individuals have brain malformations. The ATN1 gene variants that cause ... to accelerate therapeutic trials in a globally rare repeat expansion disorder. J Neurol. 2021 Aug;268(8):3031-3041. ...
    https://medlineplus.gov/genetics/gene/atn1 - Genetics
  2. MT-ATP6 gene 
    ... with Leigh syndrome. Leigh syndrome is a progressive brain disorder that usually appears in infancy or early childhood. ... decreases in cellular energy. Cell death in the brain and in other sensitive ... mitochondrial disorders is associated with the percentage of mitochondria in ...
    https://medlineplus.gov/genetics/gene/mt-atp6 - Genetics
  3. GALC gene 
    ... disease have been identified. Krabbe disease is a brain disorder that usually begins in infancy (infantile Krabbe disease) and causes movement and eating problems, impaired development, and seizures. ... myelin, nerves in the brain and other parts of the body cannot transmit ...
    https://medlineplus.gov/genetics/gene/galc - Genetics
  4. MT-ND5 gene 
    ... and some features of Leigh syndrome, a progressive brain disorder that typically appears in infancy or early childhood. ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  5. MT-ND6 gene 
    ... number of people with Leigh syndrome, a progressive brain disorder that typically appears in infancy or early childhood. ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
  6. SURF1 gene 
    ... identified in people with Leigh syndrome, a progressive brain disorder that usually appears in infancy or early childhood. Affected children may experience delayed development, muscle weakness, ... as the brain, muscles, and heart, seem especially sensitive to decreases ...
    https://medlineplus.gov/genetics/gene/surf1 - Genetics
  7. C9orf72 gene 
    ... called frontotemporal dementia (FTD), which is a progressive brain disorder that affects personality, behavior, and language. It is unclear why some people with C9orf72 gene mutations develop FTD and others do not. Individuals who develop both ... the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Brain. 2012 Mar;135(Pt 3):784-93. doi: ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  8. SDHA gene 
    ... number of people with Leigh syndrome, a progressive brain disorder that typically appears in infancy or early childhood. ...
    https://medlineplus.gov/genetics/gene/sdha - Genetics
  9. TARDBP gene 
    ... called frontotemporal dementia (FTD), which is a progressive brain disorder that affects personality, behavior, and language. It is ...
    https://medlineplus.gov/genetics/gene/tardbp - Genetics
  10. FUS gene 
    ... called frontotemporal dementia (FTD), which is a progressive brain disorder that affects personality, behavior, and language. It is ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next