Disease #04406 (EPM8 (epilepsy?, myoclonic, progressive, type 8 (EPM-8)), OMIM:616230)

Official abbreviation EPM8
Name epilepsy?, myoclonic, progressive, type 8 (EPM-8)
OMIM ID 616230
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CERS1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00334908 PME7 PubMed: Courage 2021, Journal: Courage 2021 family, 2 affected (2F) F yes - Sephardic - - - - EPM8 Sibling pair. PME7 febrile seizure at 6m. Learning difficulties noted at 3.5y. PME onset at 11y with rare TCS. Moderately severe action and rest myoclonus and ataxia from 13y. Cognitive decline. EEG: irregular GSW and polyspike + photosensitivity. PME8 normal development and early education. Memory problems noted from secondary school. Moderate myoclonus and ataxia from 16y. Rare TCS, dysarrthria. EEG: irregular GSW and polyspike + photosensitivity. - CERS1 2 2 Carolina Courage
00334910 PME8 PubMed: Courage 2021, Journal: Courage 2021 relative of PME7 F yes - Sephardic - - - - EPM8 see sib - CERS1 2 1 Carolina Courage
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