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

5 entries on 1 page. Showing entries 1 - 5.
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Phenotype details     

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Individual ID     
0000085684 short stature,developmental delay, hypotonia, feeding difficulties, inguinal/umbilical hernia,lactic acidemia, hyperammonemia, - - Familial, autosomal recessive - - - - - Hongzheng Dai 00107940
0000085685 IUGR,SGA,FTT, short stature, DD,hypotonia,feeding difficulties, lactic acidemia, hyperammonemia, dysmorphic - - Familial, autosomal recessive - - - - - Hongzheng Dai 00107941
0000122643 - - - Familial, autosomal recessive - - - - - Celia Zazo-Seco 00150101
0000220840 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 - - - 00y08m - - - - Laurent Villard 00285820
0000333045 Psychomotor retardation, cognitive impairment, seizures, spasticity, dystonia, chorea, ophthalmoparesis, bulbar signs, skeletal muscle atrophy, microcephaly, scoliosis, hypertrichosis - - Familial, autosomal recessive - - - - - Ece Sonmezler 00443771
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