| 词条 | Immunodeficiency with hyperimmunoglobulin M |
| 释义 |
| name = {{PAGENAME}} | synonyms = Hyper-IgM syndrome type 1[1] | image = X-linked recessive.svg | alt = | caption = This condition is inherited in an X-linked recessive manner | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Immunodeficiency with hyperimmunoglobulin M is a rare disorder characterized by recurrent infections, low or absent IgG, IgE, and IgA levels, and normal or elevated levels of IgM and IgD.[2]{{rp|84}} See also
References1. ^{{cite web |title=X-linked hyper-IgM syndrome |url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101088 |website=Orphanet |accessdate=18 March 2019}} 2. ^{{cite book |author1=James, William D. |author2=Berger, Timothy G. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=978-0-7216-2921-6 |oclc= |doi= |accessdate=|display-authors=etal}} External links{{Medical resources| ICD10 = D80.5 | ICD9 = | ICDO = | OMIM = 308230 | DiseasesDB = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeSH = | GeneReviewsNBK = | GeneReviewsName = | Orphanet = 101088 }}{{Cutaneous-condition-stub}} 1 : Noninfectious immunodeficiency-related cutaneous conditions |
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