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Marfan syndrome (MFS) is a multi-systemic genetic disorder that affects the connective tissue. [ 6 ] [ 7 ] [ 1 ] Those with the condition tend to be tall and thin, with long arms, legs , fingers, and toes . [ 1 ]
Marfan syndrome This page was last edited on 7 December 2024, at 09:29 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
Mare reproductive loss syndrome; Marfan syndrome; Marfanoid–progeroid–lipodystrophy syndrome; Marie Antoinette syndrome; Marinesco–Sjögren syndrome; Maroteaux–Lamy syndrome; Marshall syndrome; Marshall–Smith syndrome; Marshall–White syndrome; MASA syndrome; Mast cell activation syndrome; Mauriac syndrome; Mayer–Rokitansky ...
Antoine Bernard-Jean Marfan (French pronunciation: [ɑ̃twan bɛʁnaʁ ʒɑ̃ maʁfɑ̃]; June 23, 1858 – February 11, 1942) was a French paediatrician. He was born in Castelnaudary (département Aude , Languedoc-Roussillon ) to Antoine Prosper Marfan and Adélaïde Thuries. [ 1 ]
Marden–Walker syndrome; Marek disease; Marfan syndrome. Marfan Syndrome type II; Marfan Syndrome type III; Marfan Syndrome type IV; Marfan Syndrome type V; Marfan-like syndrome, Boileau type; Marfan-like syndrome; Marfanoid craniosynostosis syndrome; Marfanoid hypermobility; Marfanoid mental retardation syndrome autosomal; Marginal ...
Marfan syndrome - inherited as an autosomal dominant characteristic, due to mutations in the FBN1 gene that encodes fibrillin 1. [ 3 ] Homocystinuria - condition of methionine metabolism brought on by a cystathionine β-synthase deficit that causes a build-up of homocysteine and its metabolites in the urine and blood.
heart failure (undiagnosed Marfan's syndrome) 1977 [69] Heino Veskila: 22 Forward: Tartu Dünamo executed by German occupation forces during World War II 1941 [70] Ben Wilson: 17 Guard / forward: Simeon Career Academy: Class AA homicide 1984 [71] Michael Wright: 35 Power forward: Cholet: LNB Pro A: homicide 2015 [72] Olga Yakovleva: 24 Center ...
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.