Literature DB >> 7937585

Prenatal diagnosis of glutathione synthase deficiency.

N J Manning1, N P Davies, S E Olpin, K H Carpenter, M F Smith, R J Pollitt, S L Duncan, A Larsson, B Carlsson.   

Abstract

Prenatal diagnosis for glutathione synthase (EC 6.3.2.3) deficiency in two pregnancies of an at-risk couple was performed on amniotic fluid taken at 16 weeks' gestation. 5-Oxoproline (pyroglutamic acid) levels were 970 and 790 mumol/l compared with the normal mean value of 29 mumol/l (range 13-51 mumol/l). The pregnancies were terminated and the diagnosis in one case was subsequently confirmed by assay of glutathione synthase in cultured fetal fibroblasts. In the other, post-mortem tissue samples failed to grow.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7937585     DOI: 10.1002/pd.1970140611

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

Review 1.  Inborn errors in the metabolism of glutathione.

Authors:  Ellinor Ristoff; Agne Larsson
Journal:  Orphanet J Rare Dis       Date:  2007-03-30       Impact factor: 4.123

2.  Nineteen-year follow-up of a patient with severe glutathione synthetase deficiency.

Authors:  Paldeep S Atwal; Casey R Medina; Lindsay C Burrage; V Reid Sutton
Journal:  J Hum Genet       Date:  2016-03-17       Impact factor: 3.172

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.