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伊朗的埃利斯-范克里维尔德综合征:一例报告及对中东地区伊朗病例的综述

Ellis-van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East.

作者信息

Baghianimoghadam Behnam, Arabzadeh Aidin, Fallah Yousef

机构信息

Imam Khomeini Hospital Complex, Department of Orthopedic Surgery, Tehran University of Medical Sciences, Tehran, Iran.

Sina Hospital, Department of Orthopedic Surgery, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Acta Med Litu. 2021;28(2):317-324. doi: 10.15388/Amed.2021.28.2.11. Epub 2021 Aug 20.

Abstract

INTRODUCTION

Chondroectodermal dysplasia (Ellis-van Creveld syndrome (EVC)) (OMIM: 225500) is a rare skeletal dysplasia with unknown exact prevalence. EVC patients may have abnormal skeletal and extra skeletal symptoms. We report a case of EVC patient and review previous cases reported in Iran.

MATERIALS AND METHODS

The patient was a 30 years old woman referred to our hand clinic for an extra finger in both hands. She was born to a consanguineous marriage. The patient had a history of bilateral valgus deformity of the knees, for which she underwent proximal tibial and distal femoral osteotomy. Upon examination, the patient had bilateral polydactyly and brachymetacarpia with hypotrophic fingernails. She was about 120 cm tall and had acromesomelic type dwarfism. Oral examination revealed serrated incisal margins, dental transposition, a diastema, conical teeth and, enamel hypoplasia. In the radiographic examination of upper extremity, postaxial polydactyly and polymetacarpia, enlarged distal radius, and fusion of capitate and hamate were seen. We searched online databases (Pubmed, Scopus, Google Scholar) and found 14 Iranian papers with 21 reported patients (there was no time limit). We reviewed available clinical and genetic data and the geographic origins of patients.

RESULTS

14 articles reporting 22 EVC patients (including our patient) from Iran have been published in Persian and English (7 in Persian and 7 in English). All patients presented with characteristic EVC symptoms but were diagnosed at a relatively late age, 18 patients were born to consanguineous marriages.

CONCLUSIONS

It seems that based on these studies, it is possible to identify some families with this genetic mutation. We can warn such families of the dangers of consanguineous marriage through genetic counseling before marriage. In addition, by identifying families with such problems, we can detect such anomalies in the baby earlier with more careful prenatal care.

摘要

引言

软骨外胚层发育不良(埃利斯-范克里维尔德综合征(EVC))(OMIM:225500)是一种罕见的骨骼发育不良疾病,确切患病率未知。EVC患者可能有骨骼和骨骼外的异常症状。我们报告一例EVC患者,并回顾伊朗此前报道的病例。

材料与方法

该患者为一名30岁女性,因双手多指畸形转诊至我们的手部诊所。她出生于近亲结婚家庭。患者有双膝外翻畸形病史,为此接受了胫骨近端和股骨远端截骨术。检查发现,患者双手多指畸形且掌骨短小,指甲发育不良。她身高约120厘米,患有肢中短肢型侏儒症。口腔检查发现切缘呈锯齿状、牙齿异位、牙间隙、锥形牙以及釉质发育不全。上肢X线检查显示轴后多指畸形和多掌骨畸形、桡骨远端增大以及头状骨和钩骨融合。我们在在线数据库(PubMed、Scopus、谷歌学术)中进行了检索,发现了14篇伊朗文献,报道了21例患者(无时间限制)。我们回顾了现有的临床和基因数据以及患者的地理来源。

结果

已发表了14篇文章,报道了来自伊朗的22例EVC患者(包括我们的患者),文章以波斯语和英语发表(7篇波斯语,7篇英语)。所有患者均表现出典型的EVC症状,但诊断年龄相对较晚,18例患者出生于近亲结婚家庭。

结论

基于这些研究,似乎有可能识别出一些携带这种基因突变的家庭。我们可以通过婚前遗传咨询,向这些家庭警示近亲结婚的危害。此外,通过识别有此类问题的家庭,我们可以通过更仔细的产前护理,更早地在婴儿中检测到此类异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a096/8958661/f9d9e7329090/aml-28-317-g001.jpg

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