Unger S, Hecht J T
Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Ontario, Canada.
Am J Med Genet. 2001 Winter;106(4):244-50.
Pseudoachondroplasia (PSACH) (OMIM#177170) and multiple epiphyseal dysplasia (MED) are separate but overlapping osteochondrodysplasias. PSACH is a dominantly inherited disorder characterized by short-limb short stature, loose joints, and early-onset osteoarthropathy. The diagnosis is based on characteristic clinical and radiographic findings. Only mutations in the cartilage oligomeric matrix protein (COMP) gene have been reported in PSACH, and all family studies have been consistent with linkage to the COMP locus on chromosome 19. Multiple epiphyseal dysplasia (MED) is a relatively mild chondrodysplasia but like PSACH, MED causes early-onset joint degeneration, particularly of the large weight-bearing joints. Given the clinical similarity between PSACH and MED, it was not surprising that the first MED locus identified was the COMP gene (EDM1). Mutations causing MED have now been identified in five other genes (COL9A1, COL9A2, COL9A3, DTDST, and MATN3), making MED one of the most genetically heterogeneous disorders. This article reviews the clinical features of PSACH and MED, the known mutations, and the pathogenetic effect of COMP mutations on the cartilage extracellular matrix.
假性软骨发育不全(PSACH)(OMIM编号:177170)和多发性骨骺发育不良(MED)是两种不同但有重叠的骨软骨发育异常疾病。PSACH是一种常染色体显性遗传病,其特征为四肢短小、身材矮小、关节松弛以及早发性骨关节炎。诊断基于典型的临床和影像学表现。在PSACH中,仅报道了软骨寡聚基质蛋白(COMP)基因的突变,并且所有家族研究均与19号染色体上的COMP基因座连锁一致。多发性骨骺发育不良(MED)是一种相对较轻的软骨发育异常疾病,但与PSACH一样,MED会导致早发性关节退变,尤其是大的负重关节。鉴于PSACH和MED之间的临床相似性,首个被鉴定出的MED基因座是COMP基因(EDM1)也就不足为奇了。现已在其他五个基因(COL9A1、COL9A2、COL9A3、DTDST和MATN3)中鉴定出导致MED的突变,这使得MED成为遗传异质性最高的疾病之一。本文综述了PSACH和MED的临床特征、已知突变以及COMP突变对软骨细胞外基质的致病作用。