| 词条 | Mickleson syndrome |
| 释义 |
| name = Mickleson syndrome | synonyms = | image = | alt = | caption = | pronounce = | field = | geneReviewsID = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Mickleson syndrome is a very rare congenital condition that is characterized by intellectual disability and/or facial anomalies. It was first described by K.N. Mickleson in 1983.[1] References1. ^{{cite journal| title=Developmental delay, cupid's bow of the upper lip, short great toes, and skull abnormalities.| last=Mickleson| first=K. N.| year=1983| journal=Journal of clinical dysmorphology| volume=4| issue=1| pages=21–23}} External links{{Medical resources| DiseasesDB = | ICD10 = | ICD9 = | ICDO = | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = | Orphanet = 2507 }}{{Disability-stub}} 3 : Intellectual disability|Syndromes with mental retardation|Rare diseases |
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