Disease #04665 (MAE (epilepsy, myoclonic-atonic (MAE)), OMIM:616421)

Official abbreviation MAE
Name epilepsy, myoclonic-atonic (MAE)
OMIM ID 616421
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 5
Associated with 1 gene SLC6A1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00408080 188413 - - F ? Germany - - - - - MAE Seizure, Seizure precipitated by febrile infection, EEG abnormality, Hyperhidrosis, Nausea and vomiting, Generalized non-motor (absence) seizure, Myoclonic seizure SLC6A1 SLC6A1 1 1 Andreas Laner
00431864 214297 - - F no Germany - - - - - MAE Generalized non-motor (absence) seizure, Seizure, Generalized myoclonic-atonic seizure, Expressive language delay, Receptive language delay, EEG abnormality, Neurodevelopmental delay, Global developmental delay, Generalized non-motor (absence) seizure SLC6A1 SLC6A1 1 1 Andreas Laner
00435117 257545 - - M no Germany - - - - - MAE (+) Pectus excavatum,(+) Seizure,(+) Absent speech,(+) Scoliosis,(+) Neurodevelopmental delay SLC6A1 SLC6A1 1 1 Andreas Laner
00447861 283694 - - M ? ? (unknown) - - - - - MAE Neurodevelopmental delay, Intellectual disability, Autistic behavior SLC6A1 SLC6A1 1 1 Andreas Laner
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