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Concept information

disease > genetic disease > hereditary disease > Winchester syndrome
disease > complex syndrome > Winchester syndrome

Terme préférentiel

Winchester syndrome  

Définition

  • Winchester syndrome is a rare congenital connective tissue disease described in 1969, of which the main characteristics are short stature, marked contractures of joints, opacities in the cornea, coarse facial features, dissolution of the carpal and tarsal bones (in the hands and feet, respectively), and osteoporosis. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-G0RDHRV9-X

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