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syndrome de Camurati-Engelmann

См. также в других словарях:

  • 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

  • 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

  • Theodor Wilhelm Engelmann — Le professeur Engelmann. Theodor Wilhelm Engelmann (né le 14 novembre 1843 à Leipzig; † 20 mai 1909 à Berlin) est un physiologiste allemand qui a joué un rôle décisif dans l’analyse des mécanismes de la contraction musculaire et de la… …   Wikipédia en Français

  • Liste der Syndrome — Diese Seite listet in alphabetischer Reihenfolge und ohne Anspruch auf Vollständigkeit Syndrome und Komplexe aus unterschiedlichen medizinischen Fachgebieten auf. Bitte nur Verweise auf den tatsächlichen Titel des Beitrags und keine… …   Deutsch Wikipedia

  • Engleman-Camurdrie syndrome — Englemann Camurati syndrome is a rare, non fatal bone disorder that limits muscle strength.People with the Camurati Engelmann Syndrome* John Belluso, writer for the CBS television show Ghost Whisperer , was bound to a wheel chair since the age of …   Wikipedia

  • Conradi–Hünermann syndrome — Conradi Hünermann syndrome Classification and external resources ICD 10 Q77.3 ICD 9 756.59 …   Wikipedia

  • Ellis–van Creveld syndrome — Classification and external resources Polydactyly in Ellis–van Creveld syndrome ICD 10 Q …   Wikipedia

  • Craniofrontonasal syndrome — Classification and external resources OMIM 304110 Craniofrontonasal syndrome is an X linked syndrome which is more severe in females than males. Often males will have only hypertelorism (far apart eyes), whereas females have frontonasal dysplasia …   Wikipedia

  • McCune–Albright syndrome — McCune Albright syndrome Classification and external resources Café au lait skin pigmentation. A) A typical lesion on the face, chest, and arm of a 5 year old girl with McCune Albright syndrome which demonstrates jagged coast of Maine borders,… …   Wikipedia

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