| 词条 | Corneodermatoosseous syndrome |
| 释义 |
| name = Corneodermatoosseous syndrom | synonyms = | image = Autosomal dominant - en.svg | alt = | caption = This condition is inherited in an autosomal dominant manner | pronounce = | field = | geneReviewsID = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Corneodermatosseous syndrome (also known as "CDO syndrome") is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.[1] See also
References1. ^{{Fitzpatrick 6|52|513}} External links{{Medical resources| DiseasesDB = | ICD10 = H18.5 | ICD9 = | ICDO = | OMIM = 122440 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = C536444 | GeneReviewsName = | Orphanet = 3194 }}{{Cutaneous-condition-stub}} 4 : Palmoplantar keratodermas|Syndromes affecting the cornea|Syndromes with short stature|Syndromes with dysmelia |
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