Cross syndrome
Cross syndrome | |
ICD-10 | E70.3 (ILDS E70.380) |
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OMIM | 257800 |
DiseasesDB | 32011 |
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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]
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]:867-8
It was characterized in 1967.[2]It is named for Harold Cross.[3][2]
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References
- ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ↑ 2.0 2.1 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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