Osteoporosis -- oculocutaneous -- hypopigmentation syndrome: Difference between revisions
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{{SI}} | {{SI}} | ||
{{CMG}} {{AE}} {{RT}} | {{CMG}} {{AE}} {{RT}} | ||
==Overview== | ==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== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Congenital diseases]] | [[Category:Congenital diseases]] | ||
Latest revision as of 20:20, 24 July 2012
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