| 词条 | Watson syndrome |
| 释义 |
| name = Watson syndrome | synonyms = | image = | caption = | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.[1] Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.[2] 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=725, 831 |isbn=978-1-4160-2999-1 |oclc= |doi= |accessdate=}} 2. ^{{cite journal |vauthors=Allanson JE, Upadhyaya M, Watson GH, etal |title=Watson syndrome: is it a subtype of type 1 neurofibromatosis? |journal=J. Med. Genet. |volume=28 |issue=11 |pages=752–6 |date=November 1991 |pmid=1770531 |pmc=1017110 |doi=10.1136/jmg.28.11.752 |url=http://jmg.bmj.com/content/28/11/752.full.pdf }} External links{{Medical resources| DiseasesDB = 32244 | ICD10 = {{ICD10|Q|87|1|q|87}} | ICD9 = | ICDO = | OMIM = 193520 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D009456 }}{{Phakomatoses}}{{Deficiencies of intracellular signaling peptides and proteins}}{{Genodermatoses-stub}} 2 : Genodermatoses|Syndromes |
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。