Fragile X Syndrome: Prevalence, Treatment, and Prevention in China

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and the leading monogenic cause of autism spectrum disorder. Although FXS has been studied for several decades, there is relatively little basic science or clinical research being performed on FXS in China. Indeed...

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Main Authors: Niu, Manman, Han, Ying, Dy, Angel Belle C, Du, Junbao, Jin, Hongfang, Qin, Jiong, Zhang, Jing, Li, Qinrui, Hagerman, Randi J
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Published: Archīum Ateneo 2017
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Online Access:https://archium.ateneo.edu/asmph-pubs/25
https://www.frontiersin.org/articles/10.3389/fneur.2017.00254/full
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Institution: Ateneo De Manila University
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spelling ph-ateneo-arc.asmph-pubs-10242022-06-22T08:16:51Z Fragile X Syndrome: Prevalence, Treatment, and Prevention in China Niu, Manman Han, Ying Dy, Angel Belle C Du, Junbao Jin, Hongfang Qin, Jiong Zhang, Jing Li, Qinrui Hagerman, Randi J Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and the leading monogenic cause of autism spectrum disorder. Although FXS has been studied for several decades, there is relatively little basic science or clinical research being performed on FXS in China. Indeed, there is a large gap between China and Western countries in the FXS field. China has a potentially large number of FXS patients. However, many of them are underdiagnosed or even misdiagnosed, and treatments are not always administered in the Chinese population. This review discusses the prevalence, treatment, and prevention of FXS in China to facilitate an understanding of this disease in the Chinese population. 2017-06-06T07:00:00Z text https://archium.ateneo.edu/asmph-pubs/25 https://www.frontiersin.org/articles/10.3389/fneur.2017.00254/full Ateneo School of Medicine and Public Health Faculty Publications Archīum Ateneo Medicine and Health Sciences Neurology Public Health
institution Ateneo De Manila University
building Ateneo De Manila University Library
continent Asia
country Philippines
Philippines
content_provider Ateneo De Manila University Library
collection archium.Ateneo Institutional Repository
topic Medicine and Health Sciences
Neurology
Public Health
spellingShingle Medicine and Health Sciences
Neurology
Public Health
Niu, Manman
Han, Ying
Dy, Angel Belle C
Du, Junbao
Jin, Hongfang
Qin, Jiong
Zhang, Jing
Li, Qinrui
Hagerman, Randi J
Fragile X Syndrome: Prevalence, Treatment, and Prevention in China
description Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and the leading monogenic cause of autism spectrum disorder. Although FXS has been studied for several decades, there is relatively little basic science or clinical research being performed on FXS in China. Indeed, there is a large gap between China and Western countries in the FXS field. China has a potentially large number of FXS patients. However, many of them are underdiagnosed or even misdiagnosed, and treatments are not always administered in the Chinese population. This review discusses the prevalence, treatment, and prevention of FXS in China to facilitate an understanding of this disease in the Chinese population.
format text
author Niu, Manman
Han, Ying
Dy, Angel Belle C
Du, Junbao
Jin, Hongfang
Qin, Jiong
Zhang, Jing
Li, Qinrui
Hagerman, Randi J
author_facet Niu, Manman
Han, Ying
Dy, Angel Belle C
Du, Junbao
Jin, Hongfang
Qin, Jiong
Zhang, Jing
Li, Qinrui
Hagerman, Randi J
author_sort Niu, Manman
title Fragile X Syndrome: Prevalence, Treatment, and Prevention in China
title_short Fragile X Syndrome: Prevalence, Treatment, and Prevention in China
title_full Fragile X Syndrome: Prevalence, Treatment, and Prevention in China
title_fullStr Fragile X Syndrome: Prevalence, Treatment, and Prevention in China
title_full_unstemmed Fragile X Syndrome: Prevalence, Treatment, and Prevention in China
title_sort fragile x syndrome: prevalence, treatment, and prevention in china
publisher Archīum Ateneo
publishDate 2017
url https://archium.ateneo.edu/asmph-pubs/25
https://www.frontiersin.org/articles/10.3389/fneur.2017.00254/full
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