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 74 for Cerebellar agenesis
  1. Ataxia with oculomotor apraxia 
    ... of the brain involved in coordinating movements (the cerebellum) is especially at risk. It is thought that the loss of brain cells in the cerebellum causes the movement problems characteristic of ataxia with ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  2. SLC35A2-congenital disorder of glycosylation 
    ... parts of the brain called the cerebrum and cerebellum. These brain regions are necessary for thinking ability, ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  3. Spinocerebellar ataxia type 36 
    ... various parts of the brain, particularly within the cerebellum, which is the area of the brain involved ... Over time, the loss of cells in the cerebellum causes the movement problems characteristic of SCA36. In ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  4. EXOSC3 gene 
    ... of certain areas of the brain, particularly the cerebellum, which is the part of the brain that ... Minetti C, Santorelli FM. EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. J Neurol. ...
    https://medlineplus.gov/genetics/gene/exosc3 - Genetics
  5. Myoclonic epilepsy myopathy sensory ataxia 
    ... SCAE).The first symptom of MEMSA is usually cerebellar ataxia, which refers to problems with coordination and ... the brain that is involved in coordinating movement (cerebellum). Recurrent seizures (epilepsy) usually develop later, often in ...
    https://medlineplus.gov/...yoclonic-epilepsy-myopathy-sensory-ataxia - Genetics
  6. Fragile X-associated tremor/ataxia syndrome 
    ... part of the brain that controls movement (the cerebellum) and in a type of brain tissue known ... F, Ferrer E, Rivera SM. Abnormal trajectories in cerebellum and brainstem volumes in carriers of the fragile ...
    https://medlineplus.gov/...agile-x-associated-tremor-ataxia-syndrome - Genetics
  7. Charcot-Marie-Tooth disease 
    ... DISEASE, X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA; CMTX4 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  8. Schimke immuno-osseous dysplasia 
    ... Das AM, Knauth M, Becker H, Donnerstag F. Cerebellar atrophy in Schimke-immuno-osseous dysplasia. Am J ...
    https://medlineplus.gov/.../schimke-immuno-osseous-dysplasia - Genetics
  9. POLR3A gene 
    ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). ... been found in individuals with ataxia and dental abnormalities. Unlike in Pol III-related leukodystrophy (described above), ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
  10. Chiari Malformations From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Chiari Malformation/Start Here ... Chiari Malformation ... National Institute of Neurological Disorders and Stroke ... Chiari malformations (CM) are caused by problems ...
    https://www.ninds.nih.gov/.../disorders/chiari-malformations - External Health Links
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · next