| 词条 | Cross syndrome |
| 释义 |
| name = Cross syndrome | synonyms = | image = Autosomal recessive - en.svg | image_size = 150px | caption = Cross syndrome is inherited in an autosomal recessive manner | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} 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 intellectual disability and physical retardation.[1]{{rp|867–8}} It was characterized in 1967.[2] See also
References1. ^James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}. 2. ^{{cite journal |vauthors=Cross HE, McKusick VA, Breen W |title=A new oculocerebral syndrome with hypopigmentation |journal=J. Pediatr. |volume=70 |issue=3 |pages=398–406 |date=March 1967 |pmid=4959856 |doi= 10.1016/S0022-3476(67)80137-9|url=}} External links{{Medical resources| DiseasesDB = | ICD10 = E70.3 (ILDS E70.380) | ICD9 = | ICDO = | OMIM = 257800 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = | Orphanet = 2719 }}
3 : Disturbances of human pigmentation|Genetic disorders with OMIM but no gene|Rare syndromes |
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