Literature DB >> 453293

Prenatal diagnosis of Tay-Sachs disease: studies on the reliability of hexosaminidase levels in amniotic fluid.

E E Grebner, L G Jackson.   

Abstract

Measurement of hexosaminidase A activity in amniotic fluid was found to be a reliable diagnostic test in the prenatal diagnosis of Tay-Sachs disease. Including normal control specimens, analysis of 39 amniotic fluid samples have correctly predicted the condition of the fetus or, in pregnancies not yet come to term, have been in agreement with results from cultured cell extracts. In each case where both fluid and cultured cell extracts were analyzed, the results were in agreement. Analysis were performed by means of Cellogel, starch gel electrophoresis, polyacrylamide gel electrophoresis, or heat inactivation.

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Year:  1979        PMID: 453293     DOI: 10.1016/0002-9378(79)90838-x

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  2 in total

1.  Two abnormalities of hexosaminidase A in clinically normal individuals.

Authors:  E E Grebner; D A Mansfield; S S Raghavan; E H Kolodny; A d'Azzo; E F Neufeld; L G Jackson
Journal:  Am J Hum Genet       Date:  1986-04       Impact factor: 11.025

2.  Juvenile GM2 gangliosidosis (AMB variant): inability to activate hexosaminidase A by activator protein.

Authors:  K Inui; E E Grebner; L G Jackson; D A Wenger
Journal:  Am J Hum Genet       Date:  1983-07       Impact factor: 11.025

  2 in total

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