Disease #03741 (PMGYS (Polymicrogyria with seizures (PMGYS)), OMIM:614833)

Official abbreviation PMGYS
Name Polymicrogyria with seizures (PMGYS)
OMIM ID 614833
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene RTTN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00057251 - PubMed: Rump 2016 - F - Netherlands - - - - - PMGYS Microcephaly HP:0000252 - RTTN 2 2 Birgit Sikkema-Raddatz
00416847 8 PubMed: Rump 2016 sibling of patient 9 F - - - - - - - PMGYS brain magnetic resonance imaging: diffuse pachygyria; additional clinical featuresshort stature, moderate intellectual disability, bilateral metatarsus primus varus RTTN RTTN 2 1 LOVD
00416848 9 PubMed: Rump 2016 sibling of patient 8 F - - - - - - - PMGYS brain magnetic resonance imaging: mild frontal lissencephaly, posterior frontal pachygyria and parieto-occipital subcortical band heterotopia; additional clinical featuresshort stature, tetralogy of fallot, embryotoxon posterior, moderate intellectual disability (sister of patient 8) RTTN RTTN 2 1 LOVD
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