Ontology highlight
ABSTRACT:
SUBMITTER: Sihombing NRB
PROVIDER: S-EPMC7882090 | biostudies-literature | 2021 Feb
REPOSITORIES: biostudies-literature
Sihombing Nydia Rena Benita NRB Winarni Tri Indah TI Utari Agustini A van Bokhoven Hans H Hagerman Randi J RJ Faradz Sultana Mh SM
Intractable & rare diseases research 20210201 1
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 preva ...[more]