Literature DB >> 3792388

A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screening.

K J Hsiao, C H Chen, P C Chiu, S C Huang, K D Wuu.   

Abstract

A 16-year-old boy with classical phenylketonuria (PKU) and mild mental retardation (IQ 69) was detected by the screening of mentally retarded school children in Taiwan with Guthrie's bacterial inhibition assay. The follow-up family study showed that one of his married elder sisters suffered from borderline mental retardation (IQ 75) and was also diagnosed as a classical case of PKU. She had borne one boy and one girl, both suffering from mild mental retardation, microcephaly, delay in linguistic development and severe growth retardation. This is the first known Chinese family with maternal PKU. To prevent future mental retardation caused by maternal PKU, the simultaneous establishment of a register system with a neonatal screening programme, is indicated for the follow-up of PKU girls, screening of the whole family of newly discovered PKU cases, and to exclude unrecognized maternal PKU in women who have given birth to a microcephalic child.

Entities:  

Mesh:

Year:  1986        PMID: 3792388     DOI: 10.1007/bf00439250

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  16 in total

1.  STUDIES ON PHENYLKETONURIA IN A CHINESE FAMILY.

Authors:  J B TU; C C CHEN; T Y LIN; R Q BLACKWELL; Y H CHEN
Journal:  Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi       Date:  1964 Apr-Jun

2.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors:  R GUTHRIE; A SUSI
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

3.  A loophole in the phenylketonuria screening programme.

Authors:  R E Appleton; J H Baumer; J B Holton
Journal:  Lancet       Date:  1984-09-29       Impact factor: 79.321

4.  Linguistic development of children with phenylketonuria and normal intelligence.

Authors:  C R Melnick; K K Michals; R Matalon
Journal:  J Pediatr       Date:  1981-02       Impact factor: 4.406

5.  Phenylketonuria in Chinese in Singapore.

Authors:  W H Boon
Journal:  J Singapore Paediatr Soc       Date:  1978 May-Jun

6.  Maternal PKU: control of an emerging problem.

Authors:  H L Levy
Journal:  Am J Public Health       Date:  1982-12       Impact factor: 9.308

7.  Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan.

Authors:  K Tada; H Tateda; S Arashima; K Sakai; T Kitagawa; K Aoki; S Suwa; M Kawamura; T Oura; M Takesada
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

Review 8.  Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.

Authors:  F Güttler
Journal:  Acta Paediatr Scand Suppl       Date:  1980

9.  Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.

Authors:  R R Lenke; H L Levy
Journal:  N Engl J Med       Date:  1980-11-20       Impact factor: 91.245

10.  Prevention of mental retardation in offspring of hyperphenylalaninemic mothers.

Authors:  L Cartier; C L Clow; A Lippman-Hand; J Morissette; C R Scriver
Journal:  Am J Public Health       Date:  1982-12       Impact factor: 9.308

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