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. | Osteoporosis -- oculocutaneous -- hypopigmentation syndrome (OOCHS) is a rare congenital syndrome characterized by [[osteoporosis]], and reduced eye and skin pigmentation. | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Congenital diseases]] | [[Category:Congenital diseases]] | ||
Revision as of 20:15, 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.
References