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A case of brittle bone disease.
Artículo en Inglés | IMSEAR | ID: sea-1269
ABSTRACT
Brittle bone disease--synonym, osteogenesis imperfecta is a rare genetic disorder of collagen synthesis associated with broad spectrum of musculoskeletal problem, where bones break easily. Recently we got a case of OI, whose name is Babu, 3 days old, full term bay with uneventful home delivery. The baby had multiple fractures in all the extremities with deformities with blue sclera with bilateral inguinal hernia. Other systems were found normal. On 10th day of life he was operated for inguinal hernia with satisfactory postoperative recovery and subsequently he was referred to the orthopedic department for further management.
Asunto(s)
Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Osteogénesis Imperfecta / Esclerótica / Anomalías Múltiples / Humanos / Masculino / Recién Nacido / Deformidades Congénitas de las Extremidades / Fracturas Óseas / Hernia Inguinal Idioma: Inglés Año: 2004 Tipo del documento: Artículo

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Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Osteogénesis Imperfecta / Esclerótica / Anomalías Múltiples / Humanos / Masculino / Recién Nacido / Deformidades Congénitas de las Extremidades / Fracturas Óseas / Hernia Inguinal Idioma: Inglés Año: 2004 Tipo del documento: Artículo