Osteoporosis -- oculocutaneous -- hypopigmentation syndrome
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Overview
Osteoporosis -- oculocutaneous -- hypopigmentation syndrome (OOCHS) is a rare congenital syndrome characterized by osteoporosis, and reduced eye and skin pigmentation.[1]
This syndrome can be differentiated from other similar syndromes such as Cross syndrome and Preus syndrome by the absence of cerebral abnormality and presence of osteoporosis.
References