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 5
Phenotype entries for this disease 6
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

5 entries on 1 page. Showing entries 1 - 5.
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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
00472230 358911 - - M no Germany - - - - - MAE Positional foot deformity, Failure to thrive in infancy, Neurodevelopmental delay, Abnormality of the face, Abnormal skull morphology, Posteriorly rotated ears, Prominent superficial veins, Hypotonia, Delayed speech and language development, Melanocytic nevus SLC6A1 SLC6A1 1 1 Andreas Laner
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