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Results 1 - 10 of 16 for Congenital cerebellar hypoplasia
  1. Cerebellar Hypoplasia From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Cerebellar ...
    https://www.ninds.nih.gov/.../disorders/cerebellar-hypoplasia - External Health Links
  2. Pontocerebellar hypoplasia 
    Pontocerebellar hypoplasia is a group of related conditions that affect the development of the brain. The term "pontocerebellar" refers to the pons and the cerebellum, ...
    https://medlineplus.gov/.../condition/pontocerebellar-hypoplasia - Genetics
  3. Gillespie syndrome 
    Gillespie syndrome is a disorder that involves eye abnormalities, weak muscle tone from birth (congenital hypotonia), problems with balance and coordinating movements ( ...
    https://medlineplus.gov/genetics/condition/gillespie-syndrome - Genetics
  4. FKRP gene 
    ... S, Ray PN, Vajsar J. Eye and brain abnormalities in congenital muscular ... and small cerebellum prompt diagnosis of congenital muscular dystrophy due to ...
    https://medlineplus.gov/genetics/gene/fkrp - Genetics
  5. Chiari Malformations From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Chiari Malformation/Start Here ... Chiari Malformation ... Chiari malformations (CM) are caused by problems in the structure of the brain and skull. The types and ...
    https://www.ninds.nih.gov/.../disorders/chiari-malformations - External Health Links
  6. Joubert syndrome 
    ... Romani M, Micalizzi A, Valente EM. Joubert syndrome: congenital cerebellar ataxia with the molar tooth. Lancet Neurol. 2013 ...
    https://medlineplus.gov/genetics/condition/joubert-syndrome - Genetics
  7. SLC35A2-congenital disorder of glycosylation 
    ... disorder of glycosylation (SLC35A2-CDG, formerly known as congenital disorder of glycosylation type IIm) is an inherited condition that causes neurological problems and other abnormalities. This disorder's signs and symptoms and their ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  8. Walker-Warburg syndrome 
    ... buildup of fluid in the brain (hydrocephalus) or abnormalities of certain parts of the brain, including a region called the cerebellum and the part of the brain that connects ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  9. TUBB2B gene 
    ... halves of the brain (schizencephaly); or other cortical abnormalities. In some affected individuals, a region of the brain called the cerebellum is particularly affected (cerebellar dysplasia). It is thought ...
    https://medlineplus.gov/genetics/gene/tubb2b - Genetics
  10. Walking abnormalities 
    ... occurs with diabetes) Stroke or bleeding in the cerebellum Magnetic gait: Disorders that affect the front part of the brain Hydrocephalus (increased fluid in the brain)
    https://medlineplus.gov/ency/article/003199.htm - Medical Encyclopedia
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