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Lafora progressiv myoklon epilepsi
Hierarki: | ∟ ∟ ∟ ∟ Lafora progressiv myoklon epilepsi 27 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Lafora progressiv myoklon epilepsi 27 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Lafora progressiv myoklon epilepsi 27 sidobegrepp∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Anmärkning: | 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)
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historyNote*: | 2000; use Epilepsy, Myoclonic 1977-1999
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publicMeSHNote*: | 2000; see Epilepsy, Myoclonic 1977-1999
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activeMeSHYear*: | |
dateCreated*: | 1999-11-03X |
dateEstablished*: | 2000-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | KEVX |
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Termer och motsvarande begrepp: | Laforan sairaus (fi) XEpilepsia, myoklonus-, Laforan etenevä (fi, ersatt) Laforan progressiivinen myoklonusepilepsia (fi, ersatt) Laforan tauti (fi, ersatt) Progressiv myoklon epilepsi (sv, ersatt) Lafora Disease (en) Progressive Myoclonic Epilepsy, Lafora Type (en, ersatt) Progressive Myoclonic Epilepsy, Lafora (en, ersatt) Late Onset Lafora Body Disease (en, ersatt) Lafora Body Disease (en, ersatt) Lafora Progressive Myoclonic Epilepsy (en, ersatt) Lafora Type Progressive Myoclonic Epilepsy (en, ersatt) Lafora-Body Disease, Late Onset (en, ersatt) Epilepsy, Progressive Myoclonic, Lafora (en, ersatt) |
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