Camurati-Engelmann disease
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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
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
Syndrome de camurati-engelmann — Autre nom Dysplasie diaphysaire progressive Référence MIM … Wikipédia en Français
Syndrome de Camurati-Engelmann — Référence MIM 131300 Transmission Dominante Chromosome 19q13.1 Gène TGFB1 Empreinte parentale Non … Wikipédia en Français
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
Engelmann-Syndrom — Klassifikation nach ICD 10 Q78.3 Progrediente diaphysäre Dysplasie … Deutsch Wikipedia
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
Ollier disease — This article is about the disorder. For the French politician, see Patrick Ollier. Ollier disease Classification and external resources ICD 10 Q78.4 ICD 9 … Wikipedia
Chromosom 19 (Mensch) — Idiogramm des menschlichen Chromosoms 19 Chromosom 19 ist eines von 23 Chromosomen Paaren des Menschen. Ein normaler Mensch hat in den meisten seiner Zellen zwei weitgehend identische Kopien dieses Chromosoms. Inhaltsverzeichnis … Deutsch Wikipedia
CES — Contents 1 Technology 2 Medicine 3 Organization 4 People … Wikipedia
