Osteoporosis — oculocutaneous — hypopigmentation syndrome

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

↑ 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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[pmid8721572-1] 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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Osteoporosis — oculocutaneous — hypopigmentation syndrome

Overview

References

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