Oculocerebral hypopigmentation syndrome, Cross type

Oculocerebral hypopigmentation syndrome, Cross type is a rare congenital syndrome characterized by cutaneous and ocular hypopigmentation, various ocular anomalies (e.g. corneal and lens opacity, spastic ectropium, and/or nystagmus), growth deficiency, intellectual deficit and other progressive neurologic anomalies such as spastic tetraplegia, hyperreflexia, and/or athetoid movements. The clinical picture varies among patients and may also include other anomalies such as urinary tract abnormalities, Dandy-Walker malformations, and/or bilateral inguinal hernia.

Also known as: Cross syndrome, Oculocerebral Syndrome with Hypopigmentation, Kramer syndrome, hypopigmentation oculocerebral syndrome Cross type, oculocerebral hypopigmentation syndrome, oculocerebral syndrome with hypopigmentation

0 clinical trials for this condition and its sub-types, 0 tagged with Oculocerebral hypopigmentation syndrome, Cross type itself.