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华南地区43个多耳畸形病例家族的特征及463例小耳畸形患者的耳廓形态

Characteristics of 43 multiple auricular deformity case families and auricle morphology in 463 microtia patients in South China.

作者信息

Zhang Hua-Song, Chen Sui-Jun, Zeng Hai-Cang, Xiong Hao, Lin Jun-Feng, Xu Yao-Dong, Zhao Hui-Ying, Zheng Yi-Qing

机构信息

Department of Otolaryngology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China.

Institute of Hearing and Speech-Language Science, Sun Yat-sen University, Guangzhou 510120, China.

出版信息

Ann Transl Med. 2020 Apr;8(7):496. doi: 10.21037/atm.2020.03.212.

Abstract

BACKGROUND

Earlier studies have suggested that microtia is a genetic disease with a worldwide incidence of microtia is between 0.83/10,000 and 17.40/10,000. For microtia, auricle morphology is the most crucial characteristic. However, no studies have been performed to characterize the genetic similarity of microtia and auricle morphology similarity. For the sporadic patients, the relationship between the gestational age of parents and the incidence of microtia is unclear. To obtain the characteristics of auricular deformity multiple case family (AD-MCF) and clarify the relationship between genetic similarity and auricle morphology similarity in AD-MCF.

METHODS

This study included 463 AD patients who were diagnosed by Sun Yat-sen Memorial Hospital, Sun Yat-sen University, from 2013 to 2019. Among these patients, 116 are from 43 MCF and the other 347 patients are sporadic. For the patients from families, the disease status of the four generations of immediate family members and the family tree map were collected to analyze the similarity of auricle shape in family members. A score evaluated the similarity of auricle shape according to the structure of the residual ear and the similarity in the morphology of each auricle. Moreover, the population distribution of AD and the gestational age of patients were further analyzed.

RESULTS

From 2013 to 2019, a total of 463 patients were diagnosed as microtia in our hospital. There were 427 patients with unilateral disease and 36 patients with bilateral disease. Among them, 116 patients were from 34 families and 9 families. The total scores of patients in different genetic difference levels were compared and were found significantly different (P<0.001). Moreover, 58.14% of families were consistent with the law of chromosomal recessive genetic diseases. Importantly, we found that the gestational age of father in microtia families is 30.94±0.75, and mother in is 28.39±0.73 that is significantly higher than the gestational ages of parents from microtia families with P value =0.0001.

CONCLUSIONS

The auricle similarity between family members is positively related to the genetic distance between family members. The microtia patients are potentially associated with the gestational ages of parents.

摘要

背景

早期研究表明小耳症是一种遗传病,全球小耳症发病率在0.83/10000至17.40/10000之间。对于小耳症而言,耳廓形态是最关键的特征。然而,尚未有研究对小耳症的遗传相似性与耳廓形态相似性进行表征。对于散发病例,父母的孕周与小耳症发病率之间的关系尚不清楚。旨在获取耳部畸形多病例家系(AD-MCF)的特征,并阐明AD-MCF中遗传相似性与耳廓形态相似性之间的关系。

方法

本研究纳入了2013年至2019年在中山大学孙逸仙纪念医院确诊的463例AD患者。其中,116例来自43个多病例家系,其余347例为散发病例。对于来自家系的患者,收集其直系亲属四代的疾病状况和系谱图,以分析家庭成员耳廓形状的相似性。根据残余耳的结构和各耳廓形态的相似性,采用评分法评估耳廓形状的相似性。此外,进一步分析了AD的人群分布及患者的孕周。

结果

2013年至2019年,我院共诊断出463例小耳症患者。其中单侧患病427例,双侧患病36例。其中,116例患者来自34个家系和9个家族。比较了不同遗传差异水平患者的总分,发现差异有统计学意义(P<0.001)。此外,58.14%的家系符合常染色体隐性遗传病规律。重要的是,我们发现小耳症家系中父亲的孕周为30.94±0.75,母亲的孕周为28.39±0.73,显著高于非小耳症家系父母的孕周,P值=0.0001。

结论

家庭成员之间的耳廓相似性与家庭成员之间的遗传距离呈正相关。小耳症患者可能与父母的孕周有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6019/7210143/3855840eb620/atm-08-07-496-f3.jpg

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