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Results 1 - 10 of 19 for "Polymyoclonus," infantile
Did you mean "poly myoclonus," infantile?
  1. TBC1D24 gene 
    ... in people with other seizure disorders, including familial infantile myoclonic epilepsy (FIME) and progressive myoclonus epilepsy (PME). These mutations likely result in impairment ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  2. Epilepsy (National Library of Medicine)  
    Epilepsy is a brain disorder that causes people to have recurring seizures. The seizures happen when clusters of nerve cells, or neurons, in the brain send out ...
    https://medlineplus.gov/epilepsy.html - Health Topics
  3. Sialidosis 
    ... short stature, and intellectual disability. As children with infantile sialidosis type II get older, they may develop myoclonus and cherry-red spots. Other signs and symptoms ...
    https://medlineplus.gov/genetics/condition/sialidosis - Genetics
  4. CLN1 disease 
    ... individuals with this condition often have muscle twitches (myoclonus), recurrent seizures (epilepsy), and vision loss. Some affected ... older individuals develop a decline in intellectual function, myoclonus, epilepsy, and vision loss. In these individuals, life ...
    https://medlineplus.gov/genetics/condition/cln1-disease - Genetics
  5. CLN2 disease 
    ... movements (ataxia). Affected children also develop muscle twitches (myoclonus) and vision loss. CLN2 disease affects motor skills, ... symptoms of the condition. Jansky-Bielschowsky disease Late-infantile Batten disease Late-infantile neuronal ceroid lipofuscinosis LINCL ...
    https://medlineplus.gov/genetics/condition/cln2-disease - Genetics
  6. Alpers-Huttenlocher syndrome 
    ... in affected individuals can include involuntary muscle twitches (myoclonus), uncontrollable movements of the limbs (choreoathetosis), or a ... matter with hepatic cirrhosis Alpers disease Alpers progressive infantile poliodystrophy Alpers syndrome Diffuse cerebral sclerosis of Schilder ...
    https://medlineplus.gov/.../condition/alpers-huttenlocher-syndrome - Genetics
  7. Mitochondrial DNA Depletion Syndrome (Alpers' Disease) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics
    https://www.ninds.nih.gov/...s#mitochondrial-dna-depletion-syndromes - External Health Links
  8. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... Muscle Disorders/Specifics ... Muscle Disorders ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  9. Leigh Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... National Institute of Neurological ...
    https://www.ninds.nih.gov/.../mitochondrial-disorders#leigh-syndrome - External Health Links
  10. Kearns-Sayre Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Eye Diseases/Specifics ... Eye Diseases ... National Institute of Neurological Disorders and Stroke ... From ...
    https://www.ninds.nih.gov/...ondrial-disorders#kearns-sayre-syndrome - External Health Links
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