Fiedler Jörg, Bergmann Carsten, Brenner Rolf E
University of Ulm, Department of Orthopedics, Division for Biochemistry of Joint and Connective Tissue Disorders, RKU, Oberer Eselsberg 45, DE-89081 Ulm, Germany.
Acta Orthop Scand. 2003 Dec;74(6):737-41. doi: 10.1080/00016470310018298.
Spondyloepiphyseal dysplasia tarda (SEDT) is a genetically heterogeneous disorder often associated with the early onset of osteoarthrosis. The X-linked recessive form (SEDL) affects men and is characterized by reduced height, arm span exceeding total height, and barrel chest deformity. The radiographic phenotype comprises a hump-shaped deformity of vertebral bodies and mild epiphyseal dysplasia of the femoral head associated with early signs of hip arthrosis. The disorder is caused by mutations in the SEDL (or sedlin) gene on Xp22.12-p22.31. In 4 male patients from a German family, we identified a new nonsense mutation in SEDL exon 4 (C74A). The carrier status for the mutation could be confirmed in 2 women of the family, both of whom show no obvious signs of bone and joint diseases. SEDT should be kept in mind as a differential diagnosis in men with early "primary" bilateral osteoarthrosis.
迟发性脊椎骨骺发育不良(SEDT)是一种遗传异质性疾病,常与骨关节炎的早发相关。X连锁隐性形式(SEDL)影响男性,其特征为身高降低、臂展超过总身高以及桶状胸畸形。影像学表型包括椎体驼峰状畸形以及与髋关节病早期征象相关的股骨头轻度骨骺发育不良。该疾病由位于Xp22.12 - p22.31的SEDL(或sedlin)基因突变引起。在一个德国家庭的4名男性患者中,我们在SEDL外显子4中鉴定出一个新的无义突变(C74A)。该家族的2名女性被证实为该突变的携带者,她们均未表现出明显的骨关节疾病迹象。对于患有早期“原发性”双侧骨关节炎的男性,应将SEDT作为鉴别诊断予以考虑。