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Results 11 - 20 of 74 for Cerebellar agenesis
  1. Dandy-Walker malformation 
    ... the part of the skull that contains the cerebellum and the brainstem (the posterior fossa) are abnormally large. These abnormalities often result in problems with movement, coordination, intellect, ...
    https://medlineplus.gov/genetics/condition/dandy-walker-malformation - Genetics
  2. Neuronal Migration Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Brain Malformations/Specifics ... Brain Malformations ... Brain Diseases/Specifics ... Brain Diseases ... National Institute of Neurological Disorders and Stroke ... From the ...
    https://www.ninds.nih.gov/.../disorders/neuronal-migration-disorders - External Health Links
  3. Multiple System Atrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Autonomic Nervous System Disorders/Specifics ... Autonomic Nervous System Disorders ... National ...
    https://www.ninds.nih.gov/.../disorders/multiple-system-atrophy - External Health Links
  4. WASHC5 gene 
    ... syndrome because it affects craniofacial (head and face), cerebellar (brain), and cardiovascular (heart) development. People with 3C syndrome often have Dandy-Walker malformation, which is a structural abnormality of the part of the brain that coordinates ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  5. Dyskeratosis congenita 
    ... affected individuals have an unusually small and underdeveloped cerebellum, which is the part of the brain that coordinates movement. Another severe variant called Revesz syndrome involves abnormalities in the light-sensitive tissue at the back ...
    https://medlineplus.gov/genetics/condition/dyskeratosis-congenita - Genetics
  6. 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
  7. DNMT1 gene 
    ... with a nervous system disorder called autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN). Features of this disorder include difficulty coordinating movements (ataxia), hearing loss caused by abnormalities of the inner ear (sensorineural deafness), and excessive ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  8. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information ...
    https://rarediseases.info.nih.gov/diseases/7843/usher-syndrome - External Health Links
  9. Pol III-related leukodystrophy 
    ... part of the brain involved in coordinating movements (cerebellar atrophy) and underdevelopment (hypoplasia) of tissue that connects the left and right halves of the brain (the corpus callosum). These brain abnormalities likely contribute to the neurological problems in affected ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  10. Combined pituitary hormone deficiency 
    ... combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome Pituitary hormone deficiency, combined 1 Short stature-pituitary and cerebellar defects-small sella turcica syndrome National Organization for ...
    https://medlineplus.gov/.../combined-pituitary-hormone-deficiency - Genetics
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