Newborn screening for inborn errors of metabolism in Mainland China: 30 years of experience

JIMD Reports

Volumn 6, Issue , 2012, Pages 79-83

  Shi, Xiao Tong ^a   Cai, Juan ^b   Wang, Yuan Yu ^c   Tu, Wen Jun ^a   Wang, Wei Peng ^d   Gong, Li Ming ^e   Wang, Dao Wen ^f   Ye, Yin Tao ^g   Fang, Shao Guang ^h   Jing, Peng Wei ⁱ  

^a CHINA REHABILITATION RESEARCH CENTER   (China)

^b PEKING UNION MEDICAL COLLEGE   (China)

^c HEBEI MEDICAL UNIVERSITY   (China)

^d Hubei Maternal and Child Health Hospital   (China)

^e ZUNYI MEDICAL UNIVERSITY   (China)

^f Guangzhou Maternal and Child medical center ^*  (China)

^g TIANJIN MEDICAL UNIVERSITY   (China)

^h WEIFANG MEDICAL UNIVERSITY   (China)

ⁱ THE SECOND AFFILIATED HOSPITAL OF HARBIN MEDICAL UNIVERSITY   (China)

Author keywords

Congenital hypothyroidism; Methylmalonic acidemia; Newborn screen; Newborn screening; Screening center

Indexed keywords

EID: 84892443438     PISSN: 21928304     EISSN: 21928312     Source Type: Book Series    
DOI: 10.1007/8904_2011_119     Document Type: Chapter

References (6)

1. Cao Y, Yuan P, Wang YP, Mao M, Zhu J (2009) The profile of newborn screening coverage in China. J Med Screen 16(4): 163–166
2. Gu XF, Chen RG (1999) Current status of neonatal screening in China. J Med Screen 6:186–187
3. Gu XF, Wang ZJ, Ye J et al (2008) Newborn screening in China: phenylketonuria, congenital hypothyroidism and expanded screening. Ann Acad Med Singapore 37(Suppl 3):107–110
4. Padilla CD, Therrell BL (2007) Newborn screening in the Asia Pacific region. J Inherit Metab Dis 30(4):490–506
5. Zhan JY, Qin YF, Zhao ZY (2009) Neonatal screening for congenital hypothyroidism and phenylketonuria in China. World J Pediatr 5(2):136–139
6. Zheng S, Song M, Wu L, Yang S, Shen J, Lu X et al (2010) China: public health genomics. Public Health Genomics 13:269–275