Espandar Ramin, Eraghi Amir Sobhani, Mardookhpour Shirin
Department of Orthopedic, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Acta Med Iran. 2012;50(6):439-43.
Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature ageing disorder that is characterized by accelerated degenerative changes of the cutaneous, musculoskeletal and cardiovascular systems. Mean age at diagnosis is 2.9 years and generally leading to death at approximately 13 years of age due to myocardial infarction or stroke. Orthopedic manifestations of HGPS are multiple and shoulder dislocation is a rare skeletal trauma in progeria syndrome. Our patient had simultaneous shoulder and hip dislocation associated with a low energy trauma. This subject has not been reported. Treatment accomplished as close reduction under general anesthesia and immobilization.
哈钦森-吉尔福德早衰综合征(HGPS)是一种罕见的早衰性疾病,其特征为皮肤、肌肉骨骼和心血管系统加速出现退行性变化。诊断时的平均年龄为2.9岁,通常在约13岁时因心肌梗死或中风而死亡。HGPS的骨科表现多种多样,而肩关节脱位在早衰综合征中是一种罕见的骨骼创伤。我们的患者同时出现了肩关节和髋关节脱位,且与低能量创伤有关。该病例尚未见报道。治疗方法为在全身麻醉下进行闭合复位并固定。