Disease #04537 (DEE32;EIEE32 (encephalopathy, developmental and epileptic, type 32 (DEE32)), OMIM:616366)

Official abbreviation DEE32;EIEE32
Name encephalopathy, developmental and epileptic, type 32 (DEE32)
OMIM ID 616366
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene KCNA2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2022-10-21 09:28:08 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00080990 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - DEE32;EIEE32 Epileptic encephalopathy, early infantile, 32 (OMIM:616366) KCNA2 KCNA2 1 1 Daniel Trujillano
00413961 202323 - - M ? Turkey - - - - - DEE32;EIEE32 Seizure, Bilateral tonic-clonic seizure, Patchy alopecia, EEG abnormality KCNA2 KCNA2 1 1 Andreas Laner
00419668 - - - F no Russia - - - - - DEE32;EIEE32 Focal-onset seizure HP:0007359, Neurodevelopmental delay HP:0012758, Intellectual disability HP:0001249, Inability to walk HP:0002540, Hypotonia HP:0001252, Ataxia HP:0001251 KCNA2 KCNA2 1 1 Irina Romanova
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