Viljoen D
Department of Human Genetics, University of Cape Town Medical School, South Africa.
J Med Genet. 1994 Aug;31(8):640-3. doi: 10.1136/jmg.31.8.640.
Congenital contractural arachnodactyly (CCA) is an autosomal dominant disorder akin to, but usually less severe than, Marfan syndrome. The clinical features are marfanoid habitus, arachnodactyly, crumpled ears, camptodactyly of the fingers and adducted thumbs, mild contractures of the elbows, knees, and hips, and mild muscle hypoplasia especially of the calf muscles. Many patients have kyphoscoliosis and mitral valve prolapse and, very occasionally, aortic root dilatation and ectopia lentis have been described. Linkage to a gene coding for fibrillin on chromosome 5q23-31 has been shown in several kindreds. The prognosis for a normal lifespan is good and improvement in joint contractures is usual.
先天性挛缩性蜘蛛指(CCA)是一种常染色体显性疾病,与马方综合征相似,但通常症状较轻。临床特征包括类马方体型、蜘蛛指、皱缩耳、手指屈曲挛缩和拇指内收、肘部、膝部和髋部轻度挛缩,以及轻度肌肉发育不全,尤其是小腿肌肉。许多患者有脊柱后侧凸和二尖瓣脱垂,极少数情况下,曾有主动脉根部扩张和晶状体异位的描述。在几个家族中已显示与5号染色体q23 - 31上编码原纤蛋白的基因存在连锁关系。正常寿命的预后良好,关节挛缩通常会有所改善。