| 词条 | Limb–mammary syndrome |
| 释义 |
| name = Limb–mammary syndrome | synonyms = | image = | alt = | caption = | pronounce = | field = Medical genetics | geneReviewsID = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Limb–mammary syndrome is a cutaneous condition characterized by p63 mutations.[1] See also
References1. ^{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages= |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}} Further reading
External links{{Medical resources| DiseasesDB = 32743 | ICD10 = {{ICD10|Q|82|4|q|82}} | ICD9 = | ICDO = | OMIM = 603543 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = | GeneReviewsName = }}
2 : Cutaneous congenital anomalies|Syndromes affecting the skin |
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