Wilson's syndrome — Not to be confused with Wilson s disease, a rare condition caused by a defect in the body s ability to metabolize copper. Wilson’s (temperature) syndrome, also called Wilson’s thyroid syndrome or WTS, is a form of low thyroid function whose… … Wikipedia
Wilson-Mikity syndrome — Infobox Disease Name = Wilson Mikity syndrome Caption = DiseasesDB = ICD10 = ICD10|P|27|0|p|20 ICD9 = ICD9|770.7 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = In paediatrics, Wilson Mikity syndrome is a rare lung condition … Wikipedia
Wilson-Mikity syndrome — Wil·son Mik·i·ty syndrome (wilґsən mikґĭ te) [Miriam Geisendorfer Wilson, American pediatrician, born 1922; Victor G. Mikity, American radiologist, born 1919] see under syndrome … Medical dictionary
Wilson-Mikity syndrome — a rare form of pulmonary insufficiency in low birth weight infants, marked by hyperpnea and cyanosis of insidious onset during the first month of life and often resulting in death. Radiographically, there are multiple cystlike foci of… … Medical dictionary
Wilson — may refer to:People* Wilson (surname)In geography*List of peaks named Mount WilsonAustralia*Wilson, Western AustraliaCanada*Wilson Avenue (Toronto), Ontario **Wilson (TTC) subway stationPoland* Wilson Square ( Plac Wilsona ) in WarsawUnited… … Wikipedia
[hemiplegia]; wet mount; white male; white matter; whole milk; Wilson-Mikity [syndrome]; working memory — Weill Marchesani [syndrome] … Medical dictionary
Wilson's temperature syndrome — Not to be confused with Wilson s disease, a medically recognized condition caused by a defect in copper metabolism. Wilson’s (temperature) syndrome, also called Wilson’s thyroid syndrome or WTS, is an alternative medical diagnosis consisting of… … Wikipedia
Wilson's disease — Classification and external resources A Kayser Fleischer ring (the brown ring on the edge of the iris) is common in Wilson s disease, especially when neurological symptoms are present ICD … Wikipedia
Syndrome de mowat-wilson — Autre nom Maladie de Hirschsprung Retard mental Référence MIM … Wikipédia en Français
Syndrome de Mowat-Wilson — Référence MIM 235730 Transmission Dominante Chromosome 2q22 Gène ZEB2 Mutation Délétion Ponctuelle … Wikipédia en Français