Literature DB >> 25343107

Newborn screening and related policy against Phenylketonuria in China.

Lin Mei1, Peipei Song2, Lingzhong Xu1.   

Abstract

Phenylketonuria (PKU) is a treatable and preventable inherited metabolic disease. The overall incidence of PKU in China is 1/11,144. Newborn screening is an effective method of controlling PKU. In1981, the Chinese Government initiated a newborn screening program and the number of newborns screened for PKU in China has risen each year. This review describes the current status of laws and regulations related to newborn screening for PKU in China and it identifies how China's newborn screening program has improved as a result of these laws and regulations. Specific measures and regulations, such as those implemented by government, follow-up services, and government coverage of expenses, have been implemented in different areas where they have yielded good results. These measures and regulations may serve as a reference for other areas of China. However, measures and regulations regarding newborn screening in China still face challenges. Prenatal health examinations and national financial support are expected to play a more significant role in newborn screening for PKU in the future.

Entities:  

Keywords:  Phenylketonuria (PKU); incidence; inherited metabolic disease; measures and regulations; newborn screening

Year:  2013        PMID: 25343107      PMCID: PMC4204551          DOI: 10.5582/irdr.2013.v2.3.72

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  13 in total

1.  Influence of phenylalanine intake on phenylketonuria.

Authors:  H BICKEL; J GERRARD; E M HICKMANS
Journal:  Lancet       Date:  1953-10-17       Impact factor: 79.321

Review 2.  Phenylketonuria.

Authors:  Nenad Blau; Francjan J van Spronsen; Harvey L Levy
Journal:  Lancet       Date:  2010-10-23       Impact factor: 79.321

3.  Newborn screening in the Asia Pacific region.

Authors:  Carmencita D Padilla; Bradford L Therrell
Journal:  J Inherit Metab Dis       Date:  2007-07-23       Impact factor: 4.982

4.  Acute hair loss in phenylketonuria.

Authors:  A Donati; C Vincenzi; A Tosti
Journal:  J Eur Acad Dermatol Venereol       Date:  2008-08-27       Impact factor: 6.166

5.  Highlights of the new WHO Report on Newborn and Infant Hearing Screening and implications for developing countries.

Authors:  Bolajoko O Olusanya
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2011-06       Impact factor: 1.675

6.  Phenylketonuria: an inborn error of phenylalanine metabolism.

Authors:  Robin A Williams; Cyril D S Mamotte; John R Burnett
Journal:  Clin Biochem Rev       Date:  2008-02

7.  Newborn screening in China: phenylketonuria, congenital hypothyroidism and expanded screening.

Authors:  Xuefan Gu; Zhiguo Wang; Jun Ye; Lianshu Han; Wenjuan Qiu
Journal:  Ann Acad Med Singap       Date:  2008-12       Impact factor: 2.473

8.  [Retrospective study on neonatal screening for congenital hypothyroidism and phenylketonuria in China in the past 22 years].

Authors:  Yan-hua Xu; Yu-feng Qin; Zheng-yan Zhao
Journal:  Zhonghua Er Ke Za Zhi       Date:  2009-01

9.  Mutations of the phenylalanine hydroxylase gene in patients with phenylketonuria in Shanxi, China.

Authors:  Yong-An Zhou; Yun-Xia Ma; Quan-Bin Zhang; Wei-Hua Gao; Jian-Ping Liu; Jian-Ping Yang; Gai-Xiu Zhang; Xiao-Gang Zhang; Liang Yu
Journal:  Genet Mol Biol       Date:  2012-10-16       Impact factor: 1.771

10.  Cost-effectiveness analysis of neonatal hearing screening program in China: should universal screening be prioritized?

Authors:  Li-Hui Huang; Luo Zhang; Ruo-Yan Gai Tobe; Fang-Hua Qi; Long Sun; Yue Teng; Qing-Lin Ke; Fei Mai; Xue-Feng Zhang; Mei Zhang; Ru-Lan Yang; Lin Tu; Hong-Hui Li; Yan-Qing Gu; Sai-Nan Xu; Xiao-Yan Yue; Xiao-Dong Li; Bei-Er Qi; Xiao-Huan Cheng; Wei Tang; Ling-Zhong Xu; De-Min Han
Journal:  BMC Health Serv Res       Date:  2012-04-17       Impact factor: 2.655

View more
  6 in total

Review 1.  Current situation and prospects of newborn screening and treatment for Phenylketonuria in China - compared with the current situation in the United States, UK and Japan.

Authors:  Lin Mei; Peipei Song; Norihiro Kokudo; Lingzhong Xu; Wei Tang
Journal:  Intractable Rare Dis Res       Date:  2013-11

2.  Household financial burden of phenylketonuria and its impact on treatment in China: a cross-sectional study.

Authors:  Lin Wang; Hui Zou; Fang Ye; Kundi Wang; Xiaowen Li; Zhihua Chen; Jie Chen; Bingjuan Han; Weimin Yu; Chun He; Ming Shen
Journal:  J Inherit Metab Dis       Date:  2016-11-10       Impact factor: 4.982

3.  Benzene Derivatives from Ink Lead to False Positive Results in Neonatal Hyperphenylalaninemia Screening with Ninhydrin Fluorometric Method.

Authors:  Shuren Feng; Joanne Mei; Lu Yang; Ping Luo; Xiaonan Wang; Yuan Wang; Jingyi Yao; Lan Cui; Lei Pan; Zefang Wang; Li Xin
Journal:  Int J Neonatal Screen       Date:  2020-02-29

4.  Diagnostic and therapeutic recommendations for the treatment of hyperphenylalaninemia in patients 0-4 years of age.

Authors:  Ania C Muntau; Marcel du Moulin; Francois Feillet
Journal:  Orphanet J Rare Dis       Date:  2018-09-29       Impact factor: 4.123

5.  The first study of successful pregnancies in Chinese patients with Phenylketonuria.

Authors:  Lin Wang; Fang Ye; Hui Zou; Kundi Wang; Zhihua Chen; Qin Hui; Bingjuan Han; Chun He; Xiaowen Li; Ming Shen
Journal:  BMC Pregnancy Childbirth       Date:  2020-04-28       Impact factor: 3.007

6.  Challenges of Implementation of the National Phenylketonuria Screening Program in Iran: A Qualitative Study.

Authors:  Alireza Heidari; Mohammad Arab; Koorosh Etemad; Behzad Damari; Mohammad Javad Kabir
Journal:  Electron Physician       Date:  2016-10-25
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.