HOMOCYSTINURIA AND MARFAN'S SYNDROME
Author(s) -
D. P. Brenton,
Carol Dow,
J. I. P. James,
Robin Hay,
R Wynne-Davies
Publication year - 1972
Publication title -
journal of bone and joint surgery - british volume
Language(s) - English
Resource type - Journals
eISSN - 0968-7300
pISSN - 0301-620X
DOI - 10.1302/0301-620x.54b2.277
Subject(s) - homocystinuria , arachnodactyly , medicine , scoliosis , ectopia lentis , marfan syndrome , osteoporosis , genu valgum , pediatrics , surgery , genetics , amino acid , methionine , biology
1. Skeletal and other clinical features in twenty-three patients with homocystinuria have been compared with those in sixteen patients with Marfan's syndrome.2. The two diseases are clinically similar but florid arachnodactyly and scoliosis are commoner in Marfan's syndrome, whereas widening of epiphyses and metaphyses of long bones is a distinctive feature of homocystinuria.3. Patients with homocystinuria frequently have osteoporosis at a young age with a high incidence of vertebral involvement including biconcavity and flattening. Patients with Marfan's syndrome do not have osteoporosis and may have excessively tall vertebrae.4. Mental retardation and thrombosis are common in homocystinuria and uncommon in Marfan's syndrome.5. Homocystinuria is most probably inherited as an autosomal recessive and Marfan's syndrome as an autosomal dominant.6. The two diseases should be differentiated because of the thrombotic risk in homocystinuria, and also because in this disease there is a possibility of treating the...
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