Literature DB >> 1527990

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

E P Young1.   

Abstract

Twenty-four pregnancies at risk for Hurler disease (MPS I) were monitored by measurement of alpha-iduronidase in chorionic villi. Adequate samples were obtained for direct assay of the villi in 22 pregnancies. Five were found to be affected and the pregnancies were terminated. In another pregnancy an equivocal result was obtained on direct assay but analysis of the cultured chorionic cells showed the fetus to be affected. In one pregnancy where an exceptionally small biopsy was obtained, direct assay indicated the fetus to be unaffected. Following amniocentesis this result was shown to be incorrect. These results confirm that, provided an adequate sample is obtained, an accurate diagnosis can be made by direct assay of chorionic villi in pregnancies at risk for Hurler disease.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1527990     DOI: 10.1007/bf01799636

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  10 in total

1.  Variation of lysosomal enzyme activity with gestational age in chorionic villi.

Authors:  M Fukuda; A Tanaka; G Isshiki
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

Review 3.  A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome.

Authors:  C B Whitley; R J Gorlin; W Krivit
Journal:  Am J Med Genet       Date:  1987-09

4.  Chorionic villus sampling: diagnostic uses and limitations of enzyme assays.

Authors:  B Fowler; L Giles; A Cooper; I B Sardharwalla
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

5.  Comparative study of 15 lysosomal enzymes in chorionic villi and cultured amniotic fluid cells. Early prenatal diagnosis in seven pregnancies at risk for lysosomal storage diseases.

Authors:  R Gatti; C Lombardo; M Filocamo; C Borrone; E Porro
Journal:  Prenat Diagn       Date:  1985 Sep-Oct       Impact factor: 3.050

6.  Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells.

Authors:  E Young; P Willcox; A E Whitfield; A D Patrick
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

7.  Prenatal diagnosis of the Hurler syndrome: report on 40 pregnancies at risk.

Authors:  W J Kleijer; E J Thompson; M F Niermeijer
Journal:  Prenat Diagn       Date:  1983-07       Impact factor: 3.050

8.  Chromosome analysis of first trimester chorionic villus biopsies prepared by a maceration technique.

Authors:  D E Heaton; B H Czepulkowski; D H Horwell; D V Coleman
Journal:  Prenat Diagn       Date:  1984 Jul-Aug       Impact factor: 3.050

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

Authors:  J Mossman; A D Patrick
Journal:  Prenat Diagn       Date:  1982-07       Impact factor: 3.050

10.  Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells.

Authors:  R Gatti; C Borrone; M Filocamo; N Pannone; P Di Natale
Journal:  Prenat Diagn       Date:  1985 Mar-Apr       Impact factor: 3.050

  10 in total
  5 in total

1.  Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres.

Authors:  A Vellodi; E P Young; A Cooper; J E Wraith; B Winchester; C Meaney; U Ramaswami; A Will
Journal:  Arch Dis Child       Date:  1997-02       Impact factor: 3.791

Review 2.  Spinal involvement in mucopolysaccharidoses: a review.

Authors:  Antonio Leone; Donato Rigante; Daniele Zaccaria Amato; Roberto Casale; Luigi Pedone; Nicola Magarelli; Cesare Colosimo
Journal:  Childs Nerv Syst       Date:  2014-10-31       Impact factor: 1.475

Review 3.  Mucopolysaccharidoses.

Authors:  Rolando Cimaz; Francesco La Torre
Journal:  Curr Rheumatol Rep       Date:  2014-01       Impact factor: 4.592

4.  Three novel α-L-iduronidase mutations in 10 unrelated Chinese mucopolysaccharidosis type I families.

Authors:  Luning Sun; Chunyi Li; Xiaoyu Song; Ningning Zheng; Haipeng Zhang; Guizhang Dong
Journal:  Genet Mol Biol       Date:  2011-04-01       Impact factor: 1.771

5.  Mucopolysaccharidosis type I in 21 Czech and Slovak patients: mutation analysis suggests a functional importance of C-terminus of the IDUA protein.

Authors:  Alzbeta Vazna; Clare Beesley; Linda Berna; Larisa Stolnaja; Helena Myskova; Michaela Bouckova; Hana Vlaskova; Helena Poupetova; Jiri Zeman; Martin Magner; Anna Hlavata; Bryan Winchester; Martin Hrebicek; Lenka Dvorakova
Journal:  Am J Med Genet A       Date:  2009-05       Impact factor: 2.802

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.