Literature DB >> 6150236

First-trimester diagnosis of Lesch-Nyhan syndrome.

D A Gibbs, I R McFadyen, M D Crawfurd, E E De Muinck Keizer, C M Headhouse-Benson, T M Wilson, P H Farrant.   

Abstract

Chorionic villi were sampled at 8-9 weeks' gestation in four women whose fetuses were at risk for Lesch-Nyhan syndrome. Radiochemical assay of hypoxanthine phosphoribosyl transferase activity and fetal sexing (in two fetuses by means of a Y chromosome specific cDNA probe) showed that three fetuses were affected. The biochemical findings were confirmed after therapeutic abortion in two cases and spontaneous abortion in the third. Chorion biopsy and ultramicroscale enzymology may be a suitable alternative to recombinant-DNA-based methods for first-trimester diagnosis in selected diseases where the abnormal gene product is an enzyme expressed in the chorion by the 8th week of pregnancy.

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Year:  1984        PMID: 6150236     DOI: 10.1016/s0140-6736(84)92743-0

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  9 in total

1.  First trimester prenatal diagnosis of metachromatic leukodystrophy on chorionic villi by 'immunoprecipitation-electrophoresis'.

Authors:  L Poenaru; L Castelnau; A M Besançon; H Nicolesco; S Akli; D Theophil
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

Review 2.  Advances in the study of inherited metabolic disease.

Authors:  D A Gibbs
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

3.  Family studies of the Lesch-Nyhan syndrome: the use of a restriction fragment length polymorphism (RFLP) closely linked to the disease gene for carrier state and prenatal diagnosis.

Authors:  D A Gibbs; C M Headhouse-Benson; R W Watts
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Chorionic villus sampling: first trimester prenatal diagnosis.

Authors:  A T Bombard; J L Simpson; S Elias; A O Martin
Journal:  Indian J Pediatr       Date:  1986 Nov-Dec       Impact factor: 1.967

5.  Mutation analysis and prenatal diagnosis in a Lesch-Nyhan family showing non-random X-inactivation interfering with carrier detection tests.

Authors:  S Marcus; A M Steen; B Andersson; B Lambert; U Kristoffersson; U Francke
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

6.  Transferase activity function and system development process are critical in cattle embryo development.

Authors:  Heather A Adams; Bruce R Southey; Robin E Everts; Sadie L Marjani; Cindy X Tian; Harris A Lewin; Sandra L Rodriguez-Zas
Journal:  Funct Integr Genomics       Date:  2010-09-16       Impact factor: 3.410

Review 7.  Prenatal diagnosis of inborn errors of metabolism with renal manifestations.

Authors:  E Harms
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

Review 8.  A review of the molecular basis of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.

Authors:  D G Sculley; P A Dawson; B T Emmerson; R B Gordon
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

9.  Genome sequencing and protein domain annotations of Korean Hanwoo cattle identify Hanwoo-specific immunity-related and other novel genes.

Authors:  Kelsey Caetano-Anolles; Kwondo Kim; Woori Kwak; Samsun Sung; Heebal Kim; Bong-Hwan Choi; Dajeong Lim
Journal:  BMC Genet       Date:  2018-05-29       Impact factor: 2.797

  9 in total

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