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 41 - 50 of 233 for Cerebral hypoplasia
  1. TSEN2 gene 
    ... BT. Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia. Brain. 2011 Jan;134(Pt 1):143-56. doi: ...
    https://medlineplus.gov/genetics/gene/tsen2 - Genetics
  2. TSEN34 gene 
    ... BT. Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia. Brain. 2011 Jan;134(Pt 1):143-56. doi: ...
    https://medlineplus.gov/genetics/gene/tsen34 - Genetics
  3. ITM2B gene 
    ... and tissue damage in various parts of the brain. These abnormalities underlie the signs and symptoms of the familial British dementia and familial Danish dementia types of hereditary cerebral amyloid angiopathy. More About This Health Condition ABRI ...
    https://medlineplus.gov/genetics/gene/itm2b - Genetics
  4. HESX1 gene 
    ... of the pituitary gland, optic nerves, and other brain structures. These abnormalities of brain development lead to the characteristic features of septo- ...
    https://medlineplus.gov/genetics/gene/hesx1 - Genetics
  5. SETBP1 gene 
    ... impairs the expression of certain genes in the brain, disrupting development. Abnormalities in certain brain regions likely underlie the speech, intellectual, and behavioral ...
    https://medlineplus.gov/genetics/gene/setbp1 - Genetics
  6. PIK3CA gene 
    ... MCAP), which is characterized by overgrowth of the brain (megalencephaly) and abnormalities caused by enlargement of small blood vessels in ... vascular malformations, epidermal nevi, and skeletal or spinal ... the brain and can cause seizures and intellectual disability. Fibroadipose ...
    https://medlineplus.gov/genetics/gene/pik3ca - Genetics
  7. VLDLR gene 
    ... density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification. Am J Hum Genet. 2005 Sep; ... on PubMed Tissir F, Goffinet AM. Reelin and brain development. Nat ... S. Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the ...
    https://medlineplus.gov/genetics/gene/vldlr - Genetics
  8. HIVEP2 gene 
    ... alters the expression of several genes involved in brain growth and development. Abnormalities in the growth and development of the brain likely underlie the cognitive problems and other neurological ...
    https://medlineplus.gov/genetics/gene/hivep2 - Genetics
  9. TUBA1A gene 
    ... an unusually small and underdeveloped area of the brain called the cerebellum (cerebellar hypoplasia). The TUBA1A gene mutations that cause LCH change ...
    https://medlineplus.gov/genetics/gene/tuba1a - Genetics
  10. HTRA1 gene 
    ... structure of small blood vessels, particularly in the brain. These blood vessel abnormalities increase the risk of stroke and lead to the death of nerve cells (neurons) in many areas of the brain. Dysregulation of TGF-β signaling may also underlie ...
    https://medlineplus.gov/genetics/gene/htra1 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next