| 词条 | Synpolydactyly | ||||||||||||
| 释义 |
| name = Synpolydactyly | synonyms = | image = | caption = | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Synpolydactyly is a joint presentation of syndactyly (fusion of digits) and polydactyly (production of supernumerary digits). This is often a result of a mutation in the HOX D13 gene.[1] Types
References1. ^{{cite journal |vauthors=Malik S, Grzeschik KH |title=Synpolydactyly: clinical and molecular advances |journal=Clin. Genet. |volume=73 |issue=2 |pages=113–20 |date=February 2008 |pmid=18177473 |doi=10.1111/j.1399-0004.2007.00935.x }} External links{{Medical resources| DiseasesDB = 33019 | ICD10 = | ICD9 = | ICDO = | OMIM = 186000 | OMIM_mult = {{OMIM2|608180}} {{OMIM2|610234}} | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = }}{{Congenital malformations and deformations of musculoskeletal system}}{{Transcription factor deficiencies}}{{genetic-disorder-stub}} 2 : Congenital disorders of musculoskeletal system|Transcription factor deficiencies |
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