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Results 41 - 50 of 99 for Hydrocephalus
  1. Otopalatodigital syndrome type 2 
    ... increased fluid in the center of the brain (hydrocephalus), protrusion of the abdominal organs through the navel ( ...
    https://medlineplus.gov/.../otopalatodigital-syndrome-type-2 - Genetics
  2. Congenital plasminogen deficiency 
    ... buildup of this fluid in the skull (occlusive hydrocephalus). It is unclear how this feature is related ...
    https://medlineplus.gov/.../congenital-plasminogen-deficiency - Genetics
  3. Primary ciliary dyskinesia 
    ... have an accumulation of fluid in the brain (hydrocephalus), likely due to abnormal cilia in the brain. ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  4. Mucopolysaccharidosis type II 
    ... macrocephaly), a buildup of fluid in the brain (hydrocephalus), a short neck, an enlarged liver and spleen ( ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-ii - Genetics
  5. Hajdu-Cheney syndrome 
    ... balance, a buildup of fluid in the brain (hydrocephalus), abnormal breathing, and sudden death.The signs and ...
    https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome - Genetics
  6. Spina bifida 
    ... a buildup of excess fluid around the brain (hydrocephalus) and learning problems. With surgery and other forms ...
    https://medlineplus.gov/genetics/condition/spina-bifida - Genetics
  7. PTCH1 gene 
    ... L. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. Am J Med Genet ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  8. Alpha-mannosidosis 
    ... hepatosplenomegaly); a buildup of fluid in the brain (hydrocephalus); hearing loss; and a clouding of the lens ...
    https://medlineplus.gov/genetics/condition/alpha-mannosidosis - Genetics
  9. Farber lipogranulomatosis 
    ... function, a buildup of fluid in the brain (hydrocephalus), loss (atrophy) of brain tissue, paralysis of the ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  10. Transthyretin amyloidosis 
    ... brain, an accumulation of fluid in the brain (hydrocephalus), difficulty coordinating movements (ataxia), muscle stiffness and weakness ( ...
    https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis - Genetics
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