Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity
MONDO:0957267A 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.
0 clinical trials for this condition and its sub-types, 0 tagged with Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity itself.
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Tagged with Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity (0)
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