Ishida Y, Oki T, Ono Y, Nogami H
Department of Orthopaedic Surgery, Central Hospital, Aichi Prefectural Colony, Japan.
Clin Orthop Relat Res. 1992 Feb(275):144-51.
Clinical and ultrastructural study of four cases of Coffin-Lowry syndrome (CLS), a heritable disorder with peculiar facies, stooped posture, vertebral changes, and mental retardation, is reported. Three of the four cases had myelopathy caused by calcification of the ligamenta flava in early adulthood. These patients demonstrated that CLS is a calcium pyrophosphate dihydrate crystal deposition disease, and it is postulated that a metabolic abnormality in collagen and in proteoglycans are responsible for some aspects of CLS.
本文报道了4例科芬-洛里综合征(CLS)的临床和超微结构研究,该综合征是一种遗传性疾病,具有特殊面容、驼背姿势、脊柱改变和智力发育迟缓。4例中的3例在成年早期因黄韧带钙化导致脊髓病。这些患者表明CLS是一种二水焦磷酸钙晶体沉积病,据推测胶原蛋白和蛋白聚糖的代谢异常是CLS某些方面的病因。