weill���s syndrome
1Weill-Marchesani syndrome — Infobox Disease Name = PAGENAME | DiseasesDB = 29897 ICD10 = ICD9 = ICD9|759.89 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Weill Marchesani syndrome (also known as Spherophakia brachymorphia syndrome, congenital… …
2Weill-Marchesani syndrome — Weill Mar·che·sa·ni syndrome (vīlґ mahr kə sahґne) [Georges Weill, French ophthalmologist, 1866–1952; Oswald Marchesani, German ophthalmologist, 1900–1952] see under syndrome …
3Weill-Marchesani syndrome — a congenital disorder of connective tissue transmitted as an autosomal dominant or recessive trait, characterized by brachycephaly, brachydactyly, short stature with a broad chest and heavy musculature, reduced joint mobility, spherophakia,… …
4Lйri-Weill dyschondrosteosis (syndrome) — Lй·ri Weill dyschondrosteosis (syndrome) (la reґ vīlґ) [A. Lйri; Jean A. Weill, French physician, 20th century] see under dyschondrosteosis …
5Syndrome de Marfan — Référence MIM 154700 Transmission Dominante Chromosome 15q21 Gène FBN1 Mutation Ponctuelle …
6Syndrome de marfan — Autre nom {{{Autre nom}}} Référence MIM 1 …
7Syndrome MASS — Référence MIM 604308 Transmission Dominante Chromosome 15 q21 Gène FBN1 Mutation Ponctuelle Maladie généti …
8[hemiplegia]; wet mount; white male; white matter; whole milk; Wilson-Mikity [syndrome]; working memory — Weill Marchesani [syndrome] …
9syndrome — 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,… …
10Weill — Georges J., French ophthalmologist, 1866–1952. See W. Marchesani syndrome. Jean A., French physician, *1903. See Leri W. disease, Leri W. syndrome …
