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Chassaing, Nicolas; Siani, Virginie; Carles, Dominique; Delezoide, Anne Lise; Alberti, Eve Marie; Battin, Jacques; Chateil, Jean François; Gilbert-Dussardier, Brigitte; Coupry, Isabelle; Arveiler, Benoit; Saura, Robert; Lacombe, Didier
American journal of medical genetics. Part A, 1 August 2005, Volume: 136A, Issue: 4Journal Article
We describe a family with an X‐linked dominant chondrodysplasia. Four males and six females were affected through four generations. Identification of skeletal abnormalities and hydrocephaly during the pregnancy of three male fetuses led to termination of the pregnancies. A fourth affected male died at 6 days of life. The four patients had chondrodysplasia, hydrocephaly, and facial features with microphthalmia. Radiographs showed severe platyspondyly and various bone abnormalities including a distinctive metaphyseal cupping of the metacarpals, metatarsals, and phalanges. The affected females were less affected and showed small stature, sometimes associated with body asymetry and mild mental retardation. This condition appears to be a previously unrecognized X‐linked dominant chondrodysplasia. © 2005 Wiley‐Liss, Inc.
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