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一例哈钦森-吉尔福德早衰症病例报告,特别提及骨科问题。

Report on a case of Hutchinson-Gilford progeria, with special reference to orthopedic problems.

作者信息

Fernandez-Palazzi F, McLaren A T, Slowie D F

机构信息

Head Service C of Orthopedics, Hospital San Juan de Dios, Caracas, Venezuela.

出版信息

Eur J Pediatr Surg. 1992 Dec;2(6):378-82. doi: 10.1055/s-2008-1063486.

Abstract

Hutchinson-Gilford progeria is a very rare syndrome of premature aging and often features many orthopedic abnormalities. This is a case report on a young boy suffering from progeria. His orthopedic history included bilateral talus deformities of the feet, bilateral dislocated hips, pes planus, a fractured femur (which healed without complications), aseptic necrosis in the left nuclear head of the femur, bilateral fixed hip flexion deformities, bone dysplasia, osteoporosis and osteolysis.

摘要

哈钦森-吉尔福德早衰综合征是一种极为罕见的早衰综合征,常伴有许多骨科异常。这是一份关于一名患有早衰综合征的小男孩的病例报告。他的骨科病史包括双侧足距骨畸形、双侧髋关节脱位、扁平足、股骨骨折(愈合良好,无并发症)、左侧股骨头无菌性坏死、双侧固定性髋关节屈曲畸形、骨发育异常、骨质疏松和骨质溶解。

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