Myoclonic Astatic Epilepsy
What's New
Last Posted: Mar 01, 2023
- Clinical and genetic characteristics of patients with Doose syndrome.
Hinokuma Nodoka, et al. Epilepsia open 2020 0 (3) 442-450 - NBEA: Developmental disease gene with early generalized epilepsy phenotypes.
Mulhern Maureen S, et al. Annals of neurology 2018 9 - Myoclonic astatic epilepsy
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 21, 2023
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