Sihombing Nydia Rena Benita, Winarni Tri Indah, Utari Agustini, van Bokhoven Hans, Hagerman Randi J, Faradz Sultana Mh
Division of Human Genetics, Center for Biomedical Research (CEBIOR), Faculty of Medicine, Diponegoro University/Diponegoro National Hospital, Semarang, Indonesia.
Department of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia.
Intractable Rare Dis Res. 2021 Feb;10(1):11-16. doi: 10.5582/irdr.2020.03101.
Fragile X syndrome (FXS) is the most prevalent inherited cause of intellectual disability (ID) and autism spectrum disorder (ASD). Many studies have been conducted over the years, however, in Indonesia there is relatively less knowledge on the prevalence of FXS. We reviewed all studies involving FXS screening and cascade testing of the high-risk population in Indonesia for two decades, to elucidate the prevalence, as well as explore the presence of genetic clusters of FXS in Indonesia. The prevalence of FXS in the ID population of Indonesia ranged between 0.9-1.9%, while in the ASD population, the percentage was higher (6.15%). A screening and cascade testing conducted in a small village on Java Island showed a high prevalence of 45% in the ID population, suggesting a genetic cluster. The common ancestry of all affected individuals was suggestive of a founder effect in the region. Routine screening and subsequent cascade testing are essential, especially in cases of ID and ASD of unknown etiology in Indonesia.
脆性X综合征(FXS)是智力障碍(ID)和自闭症谱系障碍(ASD)最常见的遗传性病因。多年来已经开展了许多研究,然而,在印度尼西亚,关于FXS患病率的了解相对较少。我们回顾了印度尼西亚二十年来所有涉及FXS筛查和高危人群级联检测的研究,以阐明患病率,并探索印度尼西亚FXS遗传聚集情况。印度尼西亚ID人群中FXS的患病率在0.9%-1.9%之间,而在ASD人群中,该百分比更高(6.15%)。在爪哇岛一个小村庄进行的筛查和级联检测显示,ID人群中的患病率高达45%,提示存在遗传聚集。所有受影响个体的共同祖先表明该地区存在奠基者效应。常规筛查及后续的级联检测至关重要,尤其是对于印度尼西亚病因不明的ID和ASD病例。