Disease #03385 (microcephaly, postnatal progressive, with seizures and brain atrophy, OMIM:613668)

Official abbreviation -
Name microcephaly, postnatal progressive, with seizures and brain atrophy
OMIM ID 613668
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 5
Associated with 1 gene MED17
Associated tissues -
Disease features autosomal recessive
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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00150101 - - - M yes - - - - - - microcephaly, postnatal progressive, with seizures and brain atrophy - - PXDN 1 1 Celia Zazo-Seco
00285820 YL-BBZ - - F no - - - - - - microcephaly, postnatal progressive, with seizures and brain atrophy severe motor dysphasia, difficulties in chewing and swallowing, continuous drooling, accompanied by hemiparesis, microcephaly and progressive kyphoscoliosis, severe expressive speech dyspraxia, poor communication skills, could write simple words and could communicate - - 5 1 Laurent Villard
00443771 - - - F yes (Turkey) - - - - - microcephaly, postnatal progressive, with seizures and brain atrophy Psychomotor retardation, cognitive impairment, seizures, spasticity, dystonia, chorea, ophthalmoparesis, bulbar signs, skeletal muscle atrophy, microcephaly, scoliosis, hypertrichosis WDR91 WDR91 1 1 Ece Sonmezler
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