Piebald trait-neurologic defects syndrome

Piebald trait-neurologic defects syndrome is a rare, genetic, pigmentation anomaly of the skin syndrome characterized by ventral as well as dorsal leukoderma of the trunk and a congenital white forelock, in association with cerebellar ataxia, impaired motor coordination, intellectual disability of variable severity and progressive, mild to profound, uni- or bilateral sensorineural hearing loss. There have been no further descriptions in the literature since 1971.

Also known as: telfer-Sugar-Jaeger syndrome, White forelock and leukoderma with neurological impairment, piebald trait neurologic defects, piebald trait with neurologic defects, telfer Sugar Jaeger syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Piebald trait-neurologic defects syndrome itself.