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Что (кто) такое Leri-Weill syndrome - определение
HUMAN DISEASE
Leri-weill dyschondrosteosis; Leri weill dyschondrosteosis; Leri-Weill syndrome; Léri-Weill syndrome; Léri-Weill disease; Leri-Weill disease; Dyschondrosteosis; Leri-Weil syndrome; Leri Weill Syndrome; Leri-Weill dyschondrosteosis; Léri-Weill dyschondrosteosis; Leri–Weill dyschondrosteosis; Leri-Weill Dyschondrosteosis; Leri-Weil Dyschondrosteosis; Leri-Weil dyschondrosteosis
Léri–Weill dyschondrosteosis
Léri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs (mesomelic dwarfism) and a bayonet-like deformity of the forearms (Madelung's deformity).
Weill–Marchesani syndrome
AUTOSOMAL GENETIC DISEASE CHARACTERIZED BY SHORT STATURE, BACHYCEPHALY AND OTHER FACIAL ABNORMALITIES, BRACHYDACTYLY, JOINT STIFFNESS AND DISTINCTIVE OCULAR ABNORMALITIES
Weill-Marchesani syndrome; Gemss syndrome; Marchesani's syndrome; Weill-marchesani syndrome
Weill–Marchesani syndrome is a rare genetic disorder characterized by short stature; an unusually short, broad head (brachycephaly) and other facial abnormalities; hand defects, including unusually short fingers (brachydactyly); and distinctive eye (ocular) abnormalities. It was named after ophthalmologists Georges Weill (1866–1952) and Oswald Marchesani (1900–1952) who first described it in 1932 and 1939, respectively.
Étienne Weill-Raynal
FRENCH POLITICIAN (1887-1982)
Etienne Weill-Raynal
Étienne Weill-Raynal (1887–1982) was a French historian, resistant, journalist and Socialist politician. As a scholar following World War I, he specialized in the subject of reparations.
Википедия
Léri–Weill dyschondrosteosis
Léri–Weill dyschondrosteosis or LWD is a rare pseudoautosomal dominant genetic disorder which results in dwarfism with short forearms and legs (mesomelic dwarfism) and a bayonet-like deformity of the forearms (Madelung's deformity).
