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

  1. Hernández A, Nazará Z, Reynoso MC, Sarralde A, Bobadilla L, Fragoso R (1996). "Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects. A new syndrome?". Clin. Genet. 49 (1): 46–8. PMID 8721572. Unknown parameter |month= ignored (help)


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