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Results 21 - 30 of 56 for Eyelid myoclonus seizure
  1. Mitochondrial DNA Depletion Syndrome (Alpers' Disease) 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 ... Mitochondrial Diseases/Specifics
    https://www.ninds.nih.gov/...s#mitochondrial-dna-depletion-syndromes - External Health Links
  2. 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
  3. Pyridoxal phosphate-responsive seizures 
    ... The seizures typically involve irregular involuntary muscle contractions (myoclonus), abnormal eye movements, or convulsions. In some cases, the seizures may last for several minutes or the seizures ...
    https://medlineplus.gov/.../pyridoxal-phosphate-responsive-seizures - Genetics
  4. Juvenile Onset HD (Huntington's Disease Society of America) - PDF  
    Huntington's Disease/Teenagers ... Huntington's Disease ... Huntington's Disease Society of America ... PDF ... What Is Juvenile Onset Huntington's Disease (JHD)? Juvenile ...
    https://hdsa.org/.../juvenile-onset-hd - External Health Links
  5. MFSD8 gene 
    ... loss of previously acquired skills (developmental regression), recurrent seizures (epilepsy), muscle twitches (myoclonus), difficulty coordinating movements (ataxia), speech impairment, and vision ...
    https://medlineplus.gov/genetics/gene/mfsd8 - Genetics
  6. MT-TL1 gene 
    ... The features of this syndrome include muscle twitches (myoclonus), muscle weakness (myopathy), difficulty coordinating movement (ataxia), hearing loss, seizures, and diabetes.Mutations that cause MERRF/MELAS overlap ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  7. MT-TS1 gene 
    ... these cases, affected individuals typically have muscle twitches (myoclonus), muscle weakness (myopathy), difficulty coordinating movement (ataxia), hearing loss, seizures, and intellectual impairment. Two mutations in the MT- ...
    https://medlineplus.gov/genetics/gene/mt-ts1 - Genetics
  8. 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
  9. Huntington Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Huntington's Disease/Learn More ... Huntington's Disease ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and ...
    https://rarediseases.info.nih.gov/diseases/6677/huntington-disease - External Health Links
  10. CLN6 disease 
    ... developmental regression). Affected individuals can also develop recurrent seizures (epilepsy), difficulty coordinating movements (ataxia), muscle twitches (myoclonus), impaired speech (dysarthria), and vision loss. The movement ...
    https://medlineplus.gov/genetics/condition/cln6-disease - Genetics
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