View source for Osteoporosis -- oculocutaneous -- hypopigmentation syndrome

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==Overview==
Osteoporosis -- oculocutaneous -- hypopigmentation syndrome (OOCHS) is a rare congenital syndrome characterized by [[osteoporosis]], and reduced eye and skin pigmentation.<ref name="pmid8721572">{{cite journal |author=Hernández A, Nazará Z, Reynoso MC, Sarralde A, Bobadilla L, Fragoso R |title=Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects. A new syndrome? |journal=Clin. Genet. |volume=49 |issue=1 |pages=46–8 |year=1996 |month=January |pmid=8721572 |doi= |url=}}</ref>

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==
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[[Category:Disease]]
[[Category:Congenital diseases]]



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