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Up to: Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity
A neurodevelopmental disorder caused by mutation in ESAM gene. It is characterized by prenatal or neonatal onset of intracranial hemorrhage, usually with ventriculomegaly and calcifications, resulting in parenchymal brain damage.
This condition has no sub-types.