- Marfan's syndrome
- noun see Marfan syndrome
New Collegiate Dictionary. 2001.
Marfan's syndrome
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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. B. J. A. Marfan (1858 1942), French… … Medical 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
