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常染色体隐性遗传型短肢侏儒症家族中的新型临床和放射学表现

Novel Clinical and Radiological Findings in a Family with Autosomal Recessive Omodysplasia.

作者信息

Bayat Allan, Dunø Morton, Kirchhoff Maria, Jørgensen Finn S, Nishimura Gen, Hove Hanne B

机构信息

Department of Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark.

Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

出版信息

Mol Syndromol. 2020 Jun;11(2):83-89. doi: 10.1159/000506384. Epub 2020 Mar 7.

Abstract

Autosomal recessive omodysplasia (-related) is a rare short-limb skeletal dysplasia caused by biallelic mutations in the gene. Affected individuals manifest with rhizomelic short stature, decreased mobility of elbow and knee joints as well as craniofacial anomalies. Both upper and lower limbs are severely affected. These manifestations contrast with normal height and limb shortening restricted to the arms in autosomal dominant omodysplasia (-related). Here, we report 2 affected brothers of Pakistani descent from Denmark with -related omodysplasia, aiming to highlight the clinical and radiological findings. A homozygous deletion of exon 6 in the gene was detected. The pathognomonic radiological findings were distally tapered humeri and femora as well as severe proximal radioulnar diastasis. On close observations, we identified a recurrent and not previously described type of abnormal patterning in all long bones.

摘要

常染色体隐性骨发育不全(相关型)是一种罕见的短肢骨骼发育不良,由该基因的双等位基因突变引起。受影响个体表现为近端肢体短小、肘膝关节活动度降低以及颅面异常。上肢和下肢均受到严重影响。这些表现与常染色体显性骨发育不全(相关型)中身高正常且肢体缩短仅限于手臂的情况形成对比。在此,我们报告了两名来自丹麦的巴基斯坦裔患病兄弟,他们患有相关型骨发育不全,旨在突出临床和放射学表现。在该基因中检测到外显子6的纯合缺失。特征性放射学表现为肱骨和股骨远端变细以及严重的近端桡尺骨分离。通过仔细观察,我们在所有长骨中发现了一种反复出现且先前未描述过的异常模式。

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