Phenotypes for disease #03741 (PMGYS (Polymicrogyria with seizures (PMGYS)), OMIM:614833)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

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0000044550 Microcephaly HP:0000252 - - Familial, autosomal recessive - - - - - Birgit Sikkema-Raddatz 00057251
0000308357 brain magnetic resonance imaging: diffuse pachygyria; additional clinical featuresshort stature, moderate intellectual disability, bilateral metatarsus primus varus - Polymicrogyria with seizures [MIM 614833] Familial, autosomal recessive 5y - - - - LOVD 00416847
0000308358 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) - Polymicrogyria with seizures [MIM 614833] Familial, autosomal recessive 10y - - - - LOVD 00416848
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