- Leri–Weill syndrome
- Medicine: LWS (синдром Лери-Вейлля)
Универсальный русско-английский словарь. Академик.ру. 2011.
Универсальный русско-английский словарь. Академик.ру. 2011.
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
Short stature homeobox gene — or SHOX is a gene on the X chromosome and Y chromosome which is associated with short stature in humans if mutated or present in only one copy (haploinsufficiency). PathologyThe gene was first found during a search for the cause of short stature… … Wikipedia
SHOX — Short stature homeobox Isoformen SHOXA, SHOXB Bezei … Deutsch Wikipedia