Cross syndrome: Difference between revisions
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'''''Synonyms and keywords''''':Cross–McKusick–Breen syndrome, Oculocerebral-hypopigmentation syndrome, Hypopigmentation and microphthalmia | |||
==Overview== | ==Overview== |
Revision as of 20:28, 24 July 2012
Cross syndrome | |
ICD-10 | E70.3 (ILDS E70.380) |
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OMIM | 257800 |
DiseasesDB | 32011 |
WikiDoc Resources for Cross 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]
Synonyms and keywords:Cross–McKusick–Breen syndrome, Oculocerebral-hypopigmentation syndrome, Hypopigmentation and microphthalmia
Overview
Cross syndrome | |
ICD-10 | E70.3 (ILDS E70.380) |
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OMIM | 257800 |
Cross–McKusick–Breen syndrome (also known as "Cross syndrome," "Hypopigmentation and microphthalmia," and "Oculocerebral-hypopigmentation syndrome") is an extremely rare disorder characterized by white skin, blond hair with yellow-gray metallic sheen, small eyes with cloudy corneas, jerky nystagmus, gingival fibromatosis and severe mental and physical retardation.[1][2]
It was characterized in 1967.[3]It is named for Harold Cross.[4][3]
See also
External links
References
- ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ↑ Chabchoub E, Cogulu O, Durmaz B, Vermeesch JR, Ozkinay F, Fryns JP (2011). "Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29". Dermatology (Basel). 223 (4): 306–10. doi:10.1159/000335609. PMID 22327602.
- ↑ 3.0 3.1 Cross HE, McKusick VA, Breen W (1967). "A new oculocerebral syndrome with hypopigmentation". J. Pediatr. 70 (3): 398–406. doi:10.1016/S0022-3476(67)80137-9. PMID 4959856. Unknown parameter
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