Fernandez-Palazzi F, McLaren A T, Slowie D F
Head Service C of Orthopedics, Hospital San Juan de Dios, Caracas, Venezuela.
Eur J Pediatr Surg. 1992 Dec;2(6):378-82. doi: 10.1055/s-2008-1063486.
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.
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。
