Literature DB >> 6815629

Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans.

J Mossman, A D Patrick.   

Abstract

Amniotic fluid from 72 pregnancies at risk for mucopolysaccharidosis have been analysed for glycosaminoglycans (GAG) by means of two-dimensional electrophoresis. Definite results were obtained in all cases and required only 3 days to report. Of the 66 cases for which GAG analysis was accompanied by enzyme assays on cultured amniotic fluid cells, there was agreement of results in 65. In the one case of disagreement the result of GAG analysis proved to be correct. Fourteen pregnancies were predicted to be affected and the predictions were confirmed by studies on fetal tissues and/or cultured cells, or in one case the birth of an affected infant. Of the 58 pregnancies predicted to be unaffected, 48 have so far gone to term and produced healthy infants. There have been no false negative predictions. The analytical method is simple, rapid, and, in this study, has been found completely reliable to prenatal diagnosis.

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Year:  1982        PMID: 6815629     DOI: 10.1002/pd.1970020305

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


  10 in total

1.  Prenatal diagnosis of Hurler disease by analysis of alpha-iduronidase in chorionic villi.

Authors:  E P Young
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Cardiovascular studies in the mucopolysaccharidoses.

Authors:  J Nelson; M D Shields; H C Mulholland
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

Review 3.  Prenatal diagnosis of enzyme defects.

Authors:  B Winchester
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791

4.  The value of computed tomography in patients with mucopolysaccharidosis.

Authors:  J Nelson; F S Grebbell
Journal:  Neuroradiology       Date:  1987       Impact factor: 2.804

Review 5.  Prenatal diagnosis of inherited metabolic diseases.

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

6.  Mucopolysaccharidoses diagnosis in the era of enzyme replacement therapy in Egypt.

Authors:  Ekram Fateen; Zeinab Y Abdallah; Walaa S Nazim; Mona Ibrahim; Amira Radwan
Journal:  Heliyon       Date:  2021-08-19

7.  Prenatal diagnosis of Sanfilippo disease type B.

Authors:  W J Kleijer; J G Huijmans; W Blom; D Gorska; J Kubalska; M Walasek; J Zaremba
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria.

Authors:  I Mononen; V Kaartinen; T Mononen
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

9.  MPS screening methods, the Berry spot and acid turbidity tests, cause a high incidence of false-negative results in sanfilippo and morquio syndromes.

Authors:  Chang Chih-Kuang; Lin Shuan-Pei; Lee Shyue-Jye; Wang Tuen-Jen
Journal:  J Clin Lab Anal       Date:  2002       Impact factor: 2.352

Review 10.  Prenatal diagnosis of inborn errors of metabolism with renal manifestations.

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

  10 in total

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