伊朗Ellis-van Creveld综合征病例报告及中东伊朗病例回顾

Q3 Medicine Acta Medica Lituanica Pub Date : 2021-08-20 DOI:10.15388/Amed.2021.28.2.11
B. Baghianimoghadam, Aidin Arabzadeh, Yousef Fallah
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引用次数: 2

摘要

简介:软骨外胚层发育不良(Ellis–van Creveld综合征(EVC))(OMIM:#225500)是一种罕见的骨骼发育不良,确切患病率未知。EVC患者可能有异常骨骼和骨骼外症状。我们报告了一例EVC患者,并回顾了伊朗以前报告的病例。材料和方法:患者是一名30岁的女性,因双手多出一根手指而被转诊到我们的手部诊所。她出生在一个有血缘关系的婚姻中。患者有双侧膝外翻畸形病史,为此她接受了胫骨近端和股骨远端截骨。经检查,患者双侧多指和短指,指甲营养不足。她身高约120厘米,患有肢端中鼻梁型侏儒症。口腔检查显示有锯齿状切缘、牙齿移位、错位、锥形牙齿和牙釉质发育不全。上肢影像学检查可见轴后多指和多指,桡骨远端扩大,头状突和钩状突融合。我们搜索了在线数据库(Pubmed、Scopus、Google Scholar),发现了14篇伊朗论文,其中有21名报告的患者(没有时间限制)。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:用波斯语和英语发表了14篇报道22名来自伊朗的EVC患者(包括我们的患者)的文章(7篇波斯语,7篇英语)。所有患者都表现出特征性EVC症状,但在相对较晚的年龄被诊断出来,其中18名患者出生于近亲婚姻。结论:根据这些研究,似乎有可能确定一些具有这种基因突变的家庭。我们可以通过婚前基因咨询来警告这些家庭近亲结婚的危险。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发现婴儿的此类异常。
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Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
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.
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来源期刊
Acta Medica Lituanica
Acta Medica Lituanica Medicine-General Medicine
CiteScore
0.70
自引率
0.00%
发文量
33
审稿时长
16 weeks
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