Musculo-Skeletal Abnormalities in Patients with Marfan Syndrome
Author(s) -
Ali Al Kaissi,
Elisabeth Zwettler,
Rudolf Ganger,
Simone Schreiner,
Klaus Klaushofer,
Franz Grill
Publication year - 2013
Publication title -
clinical medicine insights arthritis and musculoskeletal disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.418
H-Index - 21
ISSN - 1179-5441
DOI - 10.4137/cmamd.s10279
Subject(s) - arachnodactyly , marfan syndrome , medicine , scoliosis , dysplasia , abnormality , natural history , proband , short stature , tall stature , surgery , genetics , psychiatry , mutation , gene , biology
A leptosomic body type is tall and thin with long hands. Marfanoid features may be familial in nature or pathological, as occurs in congenital contractual arachnodactyly (Beal's syndrome) and Shprintzen-Goldberg syndrome mimicking some of the changes of Marfan syndrome, although not accompanied by luxation of lens and dissecting aneurysm of aorta.
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