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Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening
by
Nguyen-Thi, My-Nuong
, Thai, Ke-Quan
, Nguyen, Huu-Trung
, Nguyen, Thuy-Vy
, Nguyen, Tuan-Anh
, Nguyen-Thi, Thanh-Truc
, Lai, Minh-Thi
, To-Mai, Xuan-Hong
in
631/208
/ 692/308
/ Autosomal recessive disorders
/ Carrier screening
/ Cross-Sectional Studies
/ Cystic fibrosis
/ Cystic Fibrosis - genetics
/ Expanded carrier screening
/ Female
/ Gene mutation
/ Genes
/ Genetic Carrier Screening - methods
/ Genetic crosses
/ Genetic screening
/ Genetic Testing - methods
/ Genetics
/ Genomics
/ Glucosephosphate dehydrogenase
/ Glycogen
/ Hearing loss
/ Hearing Loss - genetics
/ Humanities and Social Sciences
/ Humans
/ multidisciplinary
/ Mutation
/ Offspring
/ Point mutation
/ Pregnancy
/ Prevalence
/ Science
/ Science (multidisciplinary)
/ Storage diseases
/ Thalassemia
/ Vietnam - epidemiology
/ Vietnamese-specific carrier screening panel
/ Wilson's disease
/ Womens health
/ X-linked disorders
2024
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Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening
by
Nguyen-Thi, My-Nuong
, Thai, Ke-Quan
, Nguyen, Huu-Trung
, Nguyen, Thuy-Vy
, Nguyen, Tuan-Anh
, Nguyen-Thi, Thanh-Truc
, Lai, Minh-Thi
, To-Mai, Xuan-Hong
in
631/208
/ 692/308
/ Autosomal recessive disorders
/ Carrier screening
/ Cross-Sectional Studies
/ Cystic fibrosis
/ Cystic Fibrosis - genetics
/ Expanded carrier screening
/ Female
/ Gene mutation
/ Genes
/ Genetic Carrier Screening - methods
/ Genetic crosses
/ Genetic screening
/ Genetic Testing - methods
/ Genetics
/ Genomics
/ Glucosephosphate dehydrogenase
/ Glycogen
/ Hearing loss
/ Hearing Loss - genetics
/ Humanities and Social Sciences
/ Humans
/ multidisciplinary
/ Mutation
/ Offspring
/ Point mutation
/ Pregnancy
/ Prevalence
/ Science
/ Science (multidisciplinary)
/ Storage diseases
/ Thalassemia
/ Vietnam - epidemiology
/ Vietnamese-specific carrier screening panel
/ Wilson's disease
/ Womens health
/ X-linked disorders
2024
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Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening
by
Nguyen-Thi, My-Nuong
, Thai, Ke-Quan
, Nguyen, Huu-Trung
, Nguyen, Thuy-Vy
, Nguyen, Tuan-Anh
, Nguyen-Thi, Thanh-Truc
, Lai, Minh-Thi
, To-Mai, Xuan-Hong
in
631/208
/ 692/308
/ Autosomal recessive disorders
/ Carrier screening
/ Cross-Sectional Studies
/ Cystic fibrosis
/ Cystic Fibrosis - genetics
/ Expanded carrier screening
/ Female
/ Gene mutation
/ Genes
/ Genetic Carrier Screening - methods
/ Genetic crosses
/ Genetic screening
/ Genetic Testing - methods
/ Genetics
/ Genomics
/ Glucosephosphate dehydrogenase
/ Glycogen
/ Hearing loss
/ Hearing Loss - genetics
/ Humanities and Social Sciences
/ Humans
/ multidisciplinary
/ Mutation
/ Offspring
/ Point mutation
/ Pregnancy
/ Prevalence
/ Science
/ Science (multidisciplinary)
/ Storage diseases
/ Thalassemia
/ Vietnam - epidemiology
/ Vietnamese-specific carrier screening panel
/ Wilson's disease
/ Womens health
/ X-linked disorders
2024
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Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening
Journal Article
Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening
2024
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Overview
The common autosomal recessive (AR) mutation carrier is still unknown in Vietnam. This study aims to identify the most common AR gene mutation carriers in women of reproductive age to build a Vietnamese-specific carrier screening panel for AR and X-linked disorders in the preconception and prenatal healthcare program. A cross-sectional study was conducted at University Medical Center–Branch 2 in Ho Chi Minh City from December 1st, 2020, to June 30th, 2023. 338 women have consented to take a 5 mL blood test to identify 540 recessive genes. The carrier screening panel was designed based on the American College of Medical Genetics and Genomics (ACMG)-recommended genes and suggestions from 104 clinical experts in Vietnam. Obstetricians and genetic experts counseled all positive testing results to discuss the possibility of recessive diseases in their offspring. The most common recessive disorders were defined at a prevalence of 1 in 60 or greater, and those were added to a Vietnamese-specific carrier screening panel. 338 non-pregnant and pregnant women underwent the expanded carrier screening (ECS). The carrier frequency was 63.6%, in which 215 women carried at least one AR gene mutation.
GJB2
hearing impairment was identified as the most common chronic condition (1 in 5). The second most common AR disorder was beta-thalassemia (1 in 16), followed by cystic fibrosis (1 in 23), G6PD deficiency (1 in 28), Wilson’s disease (1 in 31), Usher’s syndrome (1 in 31), and glycogen storage disease (1 in 56). Seven common recessive genes were added in ethnic-based carrier screening. Women in the South of Vietnam have been carried for many recessive conditions at high frequency, such as hearing impairment, genetic anemia, and cystic fibrosis. It is necessary to implement a preconception and prenatal screening program by using seven widely popular AR genes in a Vietnamese-specific carrier screening panel to reduce the burden related to AR and X-linked disorders.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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