Genetic disorders and congenital anomalies in Nigeria: a scoping review.

IF 1.8 Q4 GENETICS & HEREDITY
Ayoade Desmond Babalola, Nitza Ferreira Muniz, Lavinia Schuler-Faccini
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Abstract

Nigeria, with its rich cultural and genetic diversity, faces a largely undocumented burden of genetic disorders and congenital anomalies. Understanding this burden is vital for effective healthcare planning and interventions. The aim of this study was to provide a comprehensive overview of the prevalence and geographical distribution of genetic disorders and congenital anomalies in Nigeria based on published evidence. A systematic scoping review was conducted across seven databases using tailored search strategies. Screening was performed in two stages: (1) title and abstract and (2) full text- prior to data extraction and analysis. Prevalence figures were recalculated and standardized as a percentage of live births or individuals. Seventy-eight studies met the inclusion criteria, of which 27 reported at least one genetic disorder. Hemoglobinopathies–particularly sickle cell disease (SCD) and sickle cell traits–were the most frequently reported conditions, with prevalence estimates as high as 61%, underscoring Nigeria’s substantial disease burden. Glucose-6-phosphate dehydrogenase (G6PD) deficiency was also commonly reported, with prevalence reaching up to 60% in some populations. Congenital anomalies involving the central nervous system, musculoskeletal system, cardiovascular system, and genitourinary tract were frequently described, with reported prevalence estimates of up to 13%, 8.8%, 3% and 6.7%, respectively. Geographically, studies were disproportionately concentrated in the southern regions, while northern areas–particularly the Northeast–were markedly underrepresented. Significant regional and condition-specific knowledge gaps persist regarding genetic disorders and congenital anomalies in Nigeria, especially in the North. Strengthening surveillance systems, expanding regionally representative research, and implementing targeted public health interventions are critical to inform equitable healthcare planning and reduce disease burden.

尼日利亚的遗传疾病和先天性异常:范围审查。
尼日利亚拥有丰富的文化和遗传多样性,但却面临着遗传疾病和先天性异常的巨大负担。了解这一负担对于有效的卫生保健规划和干预措施至关重要。本研究的目的是根据已发表的证据,全面概述尼日利亚遗传疾病和先天性异常的患病率和地理分布。使用量身定制的搜索策略对七个数据库进行了系统的范围审查。筛选分两个阶段进行:(1)标题和摘要,(2)全文-在数据提取和分析之前。患病率数据被重新计算并标准化为活产或个体的百分比。78项研究符合纳入标准,其中27项报告了至少一种遗传疾病。血红蛋白病——特别是镰状细胞病(SCD)和镰状细胞特征——是最常报告的疾病,患病率估计高达61%,突出了尼日利亚巨大的疾病负担。葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症也经常被报道,在某些人群中患病率高达60%。先天性异常包括中枢神经系统、肌肉骨骼系统、心血管系统和泌尿生殖系统,报道的患病率估计分别高达13%、8.8%、3%和6.7%。从地理上看,研究不成比例地集中在南部地区,而北部地区(尤其是东北部)的代表性明显不足。尼日利亚,特别是北部地区,在遗传疾病和先天性异常方面仍然存在重大的区域和具体情况知识差距。加强监测系统、扩大具有区域代表性的研究和实施有针对性的公共卫生干预措施,对于为公平的卫生保健规划提供信息和减轻疾病负担至关重要。
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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