Microcephaly-brain defect-spasticity-hypernatremia syndrome

Microcephaly-brain defect-spasticity-hypernatremia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterized by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatremia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. Only one familial case with three affected siblings reported and there have been no further descriptions in the literature since 1986.

Also known as: Franek-Bocker-Kahlen syndrome, microcephaly - brain defect - spasticity - hypernatremia, microcephaly brain defect spasticity hypernatremia

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly-brain defect-spasticity-hypernatremia syndrome itself.