| 词条 | Hereditary sclerosing poikiloderma |
| 释义 |
| name = Hereditary sclerosing poikiloderma | synonyms = Hereditary sclerosing poikiloderma, Weary type[1] | image = | caption = | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood.[2]{{rp|576}} See also
References1. ^{{cite web |last1=RESERVED |first1=INSERM US14-- ALL RIGHTS |title=Orphanet: Hereditary sclerosing poikiloderma, Weary type |url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=221039 |website=www.orpha.net |accessdate=15 March 2019 |language=en}} 2. ^James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. {{ISBN|0-7216-2921-0}}. External links{{Medical resources| DiseasesDB = 32778 | ICD10 = | ICD9 = | ICDO = | OMIM = 173700 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = }}{{Genodermatoses-stub}} 2 : Genodermatoses|Genetic disorders with OMIM but no gene |
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