Literature DB >> 1181074

Prenatal diagnosis of fucosidosis.

I Matsuda, S Arashima, Y Oka, T Mitsuyama, S Ariga.   

Abstract

Pregnancy from a family at risk for fucosidosis was monitored. The fetus was diagnosed as having a carrier state of the disease. alpha-L-fucosidase activity, however, was found to be absent in white blood cells obtained from identical twins after delivery. The diagnostic evaluation of (1) the enzyme activity in amniotic fluid and in cultivated amniotic fluid cells and (2) the presence of fucose rich compound in amniotic fluid are discussed.

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Year:  1975        PMID: 1181074     DOI: 10.1016/0009-8981(75)90378-2

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  4 in total

1.  Prenatal diagnosis of I-cell disease.

Authors:  I Matsuda; S Arashima; T Mitsuyama; Y Oka; T Ikeuchi; Y Kaneko; M Ishikawa
Journal:  Humangenetik       Date:  1975-10-20

2.  Restriction analysis of the structural alpha-L-fucosidase gene and its linkage to fucosidosis.

Authors:  J K Darby; P J Willems; P Nakashima; J Johnsen; R E Ferrell; E M Wijsman; D S Gerhard; N C Dracopoli; D Housman; J Henke
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

3.  Fucosidosis in a native-born Briton.

Authors:  P P Dos Santos; R W Logan
Journal:  J Clin Pathol       Date:  1977-03       Impact factor: 3.411

4.  Characterization of EcoRI mutation in fucosidosis patients: a stop codon in the open reading frame.

Authors:  K A Kretz; J K Darby; P J Willems; J S O'Brien
Journal:  J Mol Neurosci       Date:  1989       Impact factor: 3.444

  4 in total

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