MeSH 搜索器

Lafora Disease

A form of stimulus sensitive MYOCLONIC EPILEPSY inherited as an autosomal recessive condition. The most common presenting feature is a single seizure in the second decade of life. This is followed by progressive myoclonus, myoclonic seizures, tonic-clonic seizures, focal occipital seizures, intellectual decline, and severe motor and coordination impairments. Most affected individuals do not live past the age of 25 years. Concentric amyloid (Lafora) bodies are found in neurons, liver, skin, bone, and muscle (From Menkes, Textbook of Childhood Neurology, 5th ed, pp111-110).
推出的年份: 2000
副标题
树号: C10.228.140.490.375.130.650.500, C10.228.140.490.493.063.650.500, C10.574.500.529, C16.320.400.480
MeSH 单一 ID: D020192
进入的组:
  • Progressive Myoclonic Epilepsy, Lafora Type
  • Lafora Body Disease
  • Lafora Progressive Myoclonic Epilepsy
  • Lafora Type Progressive Myoclonic Epilepsy
  • Epilepsy, Progressive Myoclonic 2A
  • Lafora Body Disorder
  • Myoclonic Epilepsy of Lafora
  • Lafora Myoclonic Epilepsy
  • Epilepsy Progressive Myoclonic 2
  • Lafora Progressive Myoclonus Epilepsy
  • Progressive Myoclonic Epilepsy Type 2
  • Progressive Myoclonus Epilepsy, Lafora Type
  • Epilepsy, Progressive Myoclonic, Lafora
  • Progressive Myoclonic Epilepsy, Lafora
  • Lafora Body Disease, Late Onset
  • Late Onset Lafora Body Disease
  • Lafora-Body Disease, Late Onset
早前的内容:
  • Epilepsies, Myoclonic (1977-1999)
  • Epilepsy (1966-1976)

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