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infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly is a rare, central nervous system malformation syndrome characterized by progressive microcephaly with profound motor delay and intellectual disability, associated with hypertonia, spasticity, clonus, and seizures, with brain imaging revealing severe cerebral and cerebellar atrophy, and poor myelination.
Uniprot Description A disorder characterized by postnatal progressive microcephaly and severe developmental retardation associated with cerebral and cerebellar atrophy. Infants manifest swallowing difficulties leading to failure to thrive, jitteriness, poor visual fixation, truncal arching, seizures. There is no acquisition of developmental milestones and patients suffer from marked spasticity and profound retardation. Progressive microcephaly becomes evident few months after birth.
Mondo Term and Equivalent IDs
MONDO:0013351:  infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
DOID:0111262: 
GARD:0010995: 
Orphanet:402364: 
UMLS:C3150921: