Clinical, Phenotypic, and Demographic Characteristics of Peruvian Children and Neonates with Autosomal and Sex Chromosome Aneuploidies.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Eurasian Journal of Medicine Pub Date : 2023-02-01 DOI:10.5152/eurasianjmed.2023.22070
Jeel Moya-Salazar, Víctor Rojas-Zumaran, Rafael Vega-Vera, Eduardo Espinoza-Lecca, Hans Contreras-Pulache
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Abstract

Objective: Autosomal and sex chromosome aneuploidies are associated with multiple risk factors that determine their frequency and their social and health impact. We aimed to determine the clinical, phenotypic, and demographic characteristics of Peruvian children and neonates with autosomal and sex chromosome aneuploidies.

Materials and methods: This was a retrospective study conducted on 510 pediatric patients. We conducted a cytogenetic analysis with G-bands by trypsin using Giemsa (GTG) banding, and the results were reported using the International System for Cytogenetics Nomenclature 2013 system.

Results: Of 399 children (mean age 2.1 ± 4 years), 84 (16.47%) had aneuploidies, with 86.90% being autosomal (73.81% trisomies). In autosomal aneuploidies, 67.85% (n = 57) of the children had Down syndrome where the most common cause was free trisomy 21 (52 cases, 61.91%), followed by Robertsonian translocation (4 cases, 4.76%). Edwards and Patau syndrome affected 4 (4.76%) and 1 (1.19%) neonate. The most frequent phenotypic characteristics in children with Down syndrome were Down syndrome-like facies (45.61%) and macroglossia (19.29%). Of sex chromosome aneuploidies, 6/7 were abnormalities of the X chromosome (mainly 45,X). Neonate's age (19 ± 44.9 months), paternal age (49 ± 9 years), height (93.4 ± 176 cm), and gestational age (30 ± 15.4 weeks) were significantly correlated with the presence of sex chromosome and autosomal aneuploidies (P < .001; P = .025; and P = .001).

Conclusions: Down syndrome and Turner's syndrome were the most frequent aneuploidy and sex chromosome aneuploidy, respectively. In addition, some of the clinical, phenotypic, and demographic characteristics, such as newborn's age, paternal age, gestational age, and height, were significantly correlated with the occurrence of aneuploidy. In this sense, these characteristics could be considered risk factors among this population.

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秘鲁儿童和新生儿常染色体和性染色体非整倍体的临床、表型和人口学特征。
目的:常染色体和性染色体非整倍体与多种危险因素相关,这些因素决定了其发生频率及其对社会和健康的影响。我们的目的是确定秘鲁儿童和新生儿常染色体和性染色体非整倍体的临床、表型和人口学特征。材料和方法:本研究是一项对510例儿科患者进行的回顾性研究。采用Giemsa (GTG)带对胰蛋白酶进行g带细胞遗传学分析,并采用国际细胞遗传学命名法2013系统报告结果。结果:399例儿童(平均年龄2.1±4岁)中,非整倍体84例(16.47%),常染色体占86.90%(三体占73.81%)。在常染色体非整倍体中,67.85% (n = 57)的儿童患有唐氏综合征,其中最常见的原因是自由21三体(52例,61.91%),其次是罗伯逊易位(4例,4.76%)。爱德华兹-帕托综合征患儿4例(4.76%),1例(1.19%)。唐氏综合征患儿最常见的表型特征是唐氏综合征样相(45.61%)和大舌音(19.29%)。性染色体非整倍体中,6/7为X染色体异常(以45、X为主)。新生儿年龄(19±44.9个月)、父亲年龄(49±9岁)、身高(93.4±176 cm)、胎龄(30±15.4周)与性染色体和常染色体非整倍体存在显著相关(P < 0.001;P = 0.025;P = .001)。结论:唐氏综合征和特纳氏综合征分别是最常见的非整倍体和性染色体非整倍体。此外,一些临床、表型和人口学特征,如新生儿年龄、父亲年龄、胎龄和身高,与非整倍体的发生有显著相关。从这个意义上说,这些特征可以被认为是这一人群的危险因素。
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来源期刊
Eurasian Journal of Medicine
Eurasian Journal of Medicine Medicine-Medicine (all)
CiteScore
1.90
自引率
6.70%
发文量
59
审稿时长
16 weeks
期刊介绍: Eurasian Journal of Medicine (Eurasian J Med) is an international, scientific, open access periodical published by independent, unbiased, and triple-blinded peer-review principles. The journal is the official publication of Atatürk University School of Medicine and published triannually in February, June, and October. The publication language of the journal is English. The aim of the Eurasian Journal of Medicine is to publish original research papers of the highest scientific and clinical value in all medical fields. The Eurasian J Med also includes reviews, editorial short notes and letters to the editor that either as a comment related to recently published articles in our journal or as a case report. The target audience of the journal includes researchers, physicians and healthcare professionals who are interested or working in in all medical disciplines.
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