Literature DB >> 6711559

Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.

W Holzgreve, M S Golbus.   

Abstract

The prenatal diagnosis of ornithine transcarbamylase deficiency (OTCD) was made by using radioactive microassays for ornithine transcarbamylase (OTC) and--as an internal control--carbamyl phosphate synthetase (CPS I) in liver biopsy material from two 19-week-old at-risk fetuses. In each case, no OTC activity could be detected, while CPS I activity was normal. Control fetuses of 17-21 weeks gestation had OTC activities in the range of 10.7 to 19.4 mumol/mg protein per hr. The prenatal results were confirmed post abortum by the radiochemical assays and by an enzyme-specific cytochemical staining method.

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Year:  1984        PMID: 6711559      PMCID: PMC1684429     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  22 in total

1.  X-linked transmission of ornithine-transcarbamylase deficiency.

Authors:  C R Scott; C C Teng; S I Goodman; A Greensher; J W Mace
Journal:  Lancet       Date:  1972-11-25       Impact factor: 79.321

2.  Cytochemical demonstration of ornithine carbamoyltransferase activity in liver mitochondria of rat and mouse.

Authors:  A Mizutani
Journal:  J Histochem Cytochem       Date:  1968-03       Impact factor: 2.479

3.  Laminaria and intra-amniotic prostaglandin F2 alpha for induction of mid-trimester abortions.

Authors:  M S Golbus
Journal:  Am J Obstet Gynecol       Date:  1974-06-15       Impact factor: 8.661

4.  Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency.

Authors:  A S Goldstein; N J Hoogenraad; J D Johnson; K Fukanaga; E Swierczewski; H M Cann; P Sunshine
Journal:  Pediatr Res       Date:  1974-01       Impact factor: 3.756

5.  Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.

Authors:  P Sunshine; J E Lindenbaum; H L Levy; J M Freeman
Journal:  Pediatrics       Date:  1972-07       Impact factor: 7.124

6.  Conversion of carbamoyl phosphate to hydroxyurea. An assay for carbamoylphosphate synthetase.

Authors:  R L Levine; N Kretchmer
Journal:  Anal Biochem       Date:  1971-08       Impact factor: 3.365

7.  Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.

Authors:  I Matsuda; S Arashima; H Nambu; Y Takekoshi; M Anakura
Journal:  Pediatrics       Date:  1971-10       Impact factor: 7.124

8.  Development of urea-synthesizing enzymes in human liver.

Authors:  N C Räihä; J Suihkonen
Journal:  Acta Paediatr Scand       Date:  1968-03

9.  Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

Authors:  B Levin; J M Abraham; V G Oberholzer; E A Burgess
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

Review 10.  Enzymic differentiation in mammalian tissues.

Authors:  O Greengard
Journal:  Essays Biochem       Date:  1971       Impact factor: 8.000

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  11 in total

Review 1.  Ornithine carbamoyl transferase deficiency: findings, models and problems.

Authors:  C Bachmann
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 2.  Fetal drug metabolism and its possible clinical implications.

Authors:  B Krauer; P Dayer
Journal:  Clin Pharmacokinet       Date:  1991-07       Impact factor: 6.447

3.  Fetal tissue sampling. The San Francisco experience with 190 pregnancies.

Authors:  M S Golbus; K F McGonigle; J D Goldberg; R A Filly; P W Callen; R L Anderson
Journal:  West J Med       Date:  1989-04

4.  DNA analysis of ornithine transcarbamylase deficiency.

Authors:  U Wendel; E Wilichowski; J Schmidtke; C Bachmann
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

Review 5.  Fetal tissue sampling--indications, techniques, complications, and experience with sampling of fetal skin, liver, and muscle.

Authors:  C Cadrin; M S Golbus
Journal:  West J Med       Date:  1993-09

Review 6.  Prenatal diagnosis of inherited metabolic diseases.

Authors:  R Diukman; J D Goldberg
Journal:  West J Med       Date:  1993-09

7.  New mutation and prenatal diagnosis in ornithine transcarbamylase deficiency.

Authors:  R L Nussbaum; B A Boggs; A L Beaudet; S Doyle; J L Potter; W E O'Brien
Journal:  Am J Hum Genet       Date:  1986-02       Impact factor: 11.025

8.  Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locus.

Authors:  J E Fox; A M Hack; W A Fenton; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

9.  Prenatal exclusion of ornithine transcarbamylase (OTC) by using RFLP analysis.

Authors:  S Liechti; C Dionisi Vici; C Bachmann; M R Mazziotta; A Bartuli; G Sabetta
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

10.  DNA analysis for ornithine transcarbamylase deficiency.

Authors:  R Rozen; J E Fox; A M Hack; W A Fenton; A L Horwich; L E Rosenberg
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

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