Fiedler Jörg, Frances Anne-Marie, Le Merrer Martine, Richter Markus, Brenner Rolf E
University of Ulm, Department of Orthopedics, Ulm, Germany.
Spine (Phila Pa 1976). 2003 Nov 15;28(22):E478-82. doi: 10.1097/01.BRS.0000096667.50789.95.
Report of a family affected with X-linked spondyloepiphyseal dysplasia tarda with special respect to radiologic alterations of the spine from puberty to the forth decade and to molecular analysis of the underlying genetic defect.
To report the typical radiologic presentation of patients with X-linked spondyloepiphyseal dysplasia tarda and the diagnostic tool of mutation screening for that disease in order to avoid confusion with similar occurrences.
Spondyloepiphyseal dysplasia tarda is a genetically heterogeneous disorder that frequently manifests itself with back pain starting around puberty. The X-linked recessive form (X-linked spondyloepiphyseal dysplasia tarda) affects males and is clinically characterized by an arm span markedly exceeding total height, a barrel chest deformity, and early development of degenerative joint disease. The disorder is caused by mutations in the SEDL gene located on Xp22.12-p22.31.
Radiologic alterations of the cervical, thoracal, and lumbar spine were assessed in the affected family members and one suspected female carrier in correlation to age. All 6 exon codings for the SEDL gene were analyzed by primer cycle sequencing.
In 3 male patients from a French family, we identified a 5 base pair deletion in SEDL, exon 5 at position 267-271 (delAAGAC). Carrier status for the mutation could be confirmed in one female member of the family, which is inconspicuous in terms of spine and joint diseases. Radiologic abnormalities of the patients comprised generalized platyspondyly, a hump-shaped deformity of cervical, thoracal, and lumbar vertebral bodies as well as signs of retrospondylophytes, osteochondrosis, and spondylarthrosis.
X-linked spondyloepiphyseal dysplasia tarda should be kept in mind as a differential diagnosis in men with early onset of back pain and radiologic abnormalities of the vertebral bodies comprising platyspondyly and a central hump.
关于一个患有迟发性X连锁脊椎骨骺发育不良的家族报告,特别关注从青春期到四十岁期间脊柱的放射学改变以及潜在基因缺陷的分子分析。
报告迟发性X连锁脊椎骨骺发育不良患者的典型放射学表现以及该病的突变筛查诊断工具,以避免与类似病症混淆。
迟发性脊椎骨骺发育不良是一种基因异质性疾病,常于青春期左右开始出现背痛症状。X连锁隐性形式(迟发性X连锁脊椎骨骺发育不良)影响男性,临床特征为臂展明显超过身高、桶状胸畸形以及退行性关节病的早期发展。该疾病由位于Xp22.12 - p22.31的SEDL基因突变引起。
对受影响的家族成员和一名疑似女性携带者的颈椎、胸椎和腰椎的放射学改变进行与年龄相关的评估。通过引物循环测序分析SEDL基因的所有6个外显子编码。
在一个法国家族的3名男性患者中,我们在SEDL基因第5外显子267 - 271位发现一个5碱基对缺失(delAAGAC)。该家族的一名女性成员被证实为该突变的携带者,其在脊柱和关节疾病方面无明显症状。患者的放射学异常包括全身性椎体扁平、颈椎、胸椎和腰椎椎体呈驼峰状畸形以及脊柱后骨赘、骨软骨病和脊椎关节病的迹象。
对于早期出现背痛且椎体有包括椎体扁平及中央驼峰在内的放射学异常的男性,应考虑迟发性X连锁脊椎骨骺发育不良作为鉴别诊断。