Léri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs (mesomelic...

malformed wrists and wrist bones and is often associated with Léri-Weill dyschondrosteosis. It can be bilateral (in both wrists) or just in the one wrist...

XXY, 47,XYY, etc.). Deletions have also been associated with Léri-Weill dyschondrosteosis and Madelung's deformity. Interleukin-3 receptor Interleukin-9...

mesomelic dysplasia Ellis–van Creveld syndrome Robinow syndrome Léri–Weill dyschondrosteosis "mesomelia". The American Heritage® Medical Dictionary. Retrieved...

Leptomeningeal capillary - venous angiomatosis Leptospirosis Leri pleonosteosis Léri–Weill dyschondrosteosis Lesch–Nyhan syndrome Lethal chondrodysplasia Moerman...

gene has been found to play a role in idiopathic short stature, Léri-Weill dyschondrosteosis, and Langer mesomelic dysplasia. Gene dosage effects of extra...

Conradi–Hünermann syndrome Other dwarfism Fibrochondrogenesis Short rib – polydactyly syndrome Majewski's polydactyly syndrome Léri–Weill dyschondrosteosis...

deformed forearms, which was to become known as Léri-Weill dyschondrosteosis. With Pierre Marie, the "Marie-Léri syndrome" is named, which is a hand disorder...

Carrying only one mutant allele (heterozygosity) presents as Léri–Weill dyschondrosteosis. Mutations of the enhancer regions may be connected to less severe...

151100; PTPN11 Leprechaunism; 246200; INSR Léri–Weill dyschondrosteosis; 127300; SHOX Leri–Weill dyschondrosteosis; 127300; SHOXY Lesch–Nyhan syndrome; 300322;...