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Medicine Today. 2007; 5 (1): 25-27
de En | IMEMR | ID: emr-84484
Bibliothèque responsable: EMRO
Osteogenesis imperfecta [OI] is a heritable disease of bone the hallmark of which is bone fragility. It is an autosomal dominant disorder. Diagnosis is usually clinical, based mainly on typical features. There is no curative treatment for OI. Active physical rehabilitation in the early years allows children to attain a higher functional level than does orthopaedic management alone. Therefore family physicians need to play an active role in guiding their patients to optimal rehabilitation
Sujet(s)
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Indice: IMEMR Sujet Principal: Ostéogenèse imparfaite / Dysplasies osseuses / Anomalies morphologiques congénitales des membres / Muscles squelettiques / Conseil génétique / Nourrisson Limites du sujet: Humans / Male langue: En Texte intégral: Med. Today Année: 2007
Recherche sur Google
Indice: IMEMR Sujet Principal: Ostéogenèse imparfaite / Dysplasies osseuses / Anomalies morphologiques congénitales des membres / Muscles squelettiques / Conseil génétique / Nourrisson Limites du sujet: Humans / Male langue: En Texte intégral: Med. Today Année: 2007