syndrome de Leri-Weill
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syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Weill — Georges J., French ophthalmologist, 1866–1952. See W. Marchesani syndrome. Jean A., French physician, *1903. See Leri W. disease, Leri W. syndrome … Medical dictionary
Leri — André, French orthopedic surgeon, 1875–1930. See L. pleonosteosis, L. sign, L. Weill disease, L. Weill syndrome … Medical dictionary
André Léri — (1875 September 8, 1930} was a French neurologist who was born in Paris. He received he doctorate in 1904 from the University of Paris where he studied under Joseph Babinski (1857 1932) and Pierre Marie (1853 1940). During World War I, Léri was… … 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
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
Maffucci syndrome — Classification and external resources ICD 10 Q78.4 ICD 9 756.4 … Wikipedia
Majewski's polydactyly syndrome — Classification and external resources OMIM 263520 DiseasesDB 32793 Majewski s polydactyly syndrome, also known as polydactyly with neonata … Wikipedia
Pathologies en rapport avec une haploinsuffisance du gene SHOX — Pathologies en rapport avec une haploinsuffisance du gène SHOX Pathologies en rapport avec une haploinsuffisance du gène SHOX Autre nom {{{Autre nom}}} Référence MIM … Wikipédia en Français
Pathologies en rapport avec une haploinsuffisance du gène SHOX — Référence MIM 127300 Transmission Dominante Chromosome Xpter p22.32 Ypter p11.2 Gène SHOX SHOXY Mutation … Wikipédia en Français
