Medical dictionary. 2011.
Marfan's syndrome — noun see Marfan syndrome … New Collegiate Dictionary
Marfan's syndrome — [ mα:faMarfan s syndromez] noun Medicine a hereditary disorder of the connective tissue, resulting in abnormally long and thin digits and also frequently in optical and cardiovascular defects. Origin 1930s: named after the French paediatrician… … English new terms dictionary
Marfan's syndrome — an inherited disorder of connective tissue characterized by excessive tallness, abnormally long and slender fingers and toes (arachnodactyly), heart defects, and partial dislocation of the lenses of the eyes [J. A. Marfan (1858–1942), French… … The new mediacal dictionary
Marfan's syndrome — noun an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system • Hypernyms: ↑autosomal dominant disease, ↑autosomal dominant disorder … Useful english dictionary
Marfan syndrome — Marfan redirects here. For the person after whom the syndrome is named, see Antoine Marfan. Marfan syndrome Classification and external resources Micrograph demonstrating myxomatous degeneration of the aorti … Wikipedia
Syndrome de Marfan — Référence MIM 154700 Transmission Dominante Chromosome 15q21 Gène FBN1 Mutation Ponctuelle … Wikipédia en Français
Syndrome de marfan — Autre nom {{{Autre nom}}} Référence MIM 1 … Wikipédia en Français
Marfan syndrome — [mär′fan] n. [after Antonin Marfan (1858 1942), Fr physician, who first described it (1892)] a hereditary disorder characterized by abnormalities of the blood circulation and the eyes, abnormally long bones in the limbs, and very mobile joints:… … English World dictionary
Syndrome de loeys-dietz — Autre nom {{{Autre nom}}} Référence MIM … Wikipédia en Français
Syndrome de Loeys-Dietz — Référence MIM 609192 Transmission Dominante Chromosome 9 3 q33 q34 p22 Gène TGFBR1 TGFBR2 Mutation Ponctuel … Wikipédia en Français
