Engelmann disease
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Engelmann disease — Eng·el·mann disease (engґgəl mahn) [Guido Engelmann, Austrian orthopedic surgeon, 1876–1959] diaphyseal dysplasia … Medical dictionary
Camurati-Engelmann disease — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 4301 ICD10 = ICD10|Q|78|3|q|65 ICD9 = ICD9|756.59 ICDO = OMIM = 131300 OMIM mult = OMIM2|606631 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D003966Camurati Engelmann Disease (CED) … Wikipedia
Engelmann syndrome — is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton.cite journal author=Janssens K, Vanhoenacker F, Bonduelle M, et al title=Camurati Engelmann disease: review of the clinical, radiological, and … Wikipedia
Camurati-Engelmann disease — Cam·u·ra·ti En·gel·mann disease (kah moo rahґte engґgəl mahn) [Mario Camurati, Italian physician, 1896–1948; Guido Engelmann, Czechoslovakian surgeon, 20th century] diaphyseal dysplasia … Medical dictionary
Engelmann-Syndrom — Klassifikation nach ICD 10 Q78.3 Progrediente diaphysäre Dysplasie … Deutsch Wikipedia
Camurati-Engelmann disease — diaphyseal dysplasia … Medical dictionary
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
Engelmann — Guido, German surgeon, *1876. See E. disease. Theodor W., German physiologist, 1843–1909. See E. basal knobs, under knob … Medical dictionary
Syndrome de camurati-engelmann — Autre nom Dysplasie diaphysaire progressive Référence MIM … Wikipédia en Français
Hirschsprung's disease — Classification and external resources Histopathology of Hirschsprung disease. Enzyme histochemistry showing aberrant acetylcholine esterase (ACHE) positive fibres (brown) in the lamina propria mucosae … Wikipedia
