Literature DB >> 414620

Carrier detection in Sandhoff disease.

J A Lowden, E J Ives, D L Keene, A L Burton, M A Skomorowski, F Howard.   

Abstract

Three new cases of Sandhoff disease are reported. One infant was the second affected child in a large family. The parents, who were cousins, were part of a large kindred from an isolated community in northern Saskatchewan. We assayed total and heat-stable hexosaminidases in 38 other members of the kindred and found two distinct cohorts. Sixteen individuals had low total and low heat-stable hexosaminidase and were diagnosed as carriers of Sandhoff disease. The values for the remainder were within normal limits. In a retrospective study of data from more than 14,000 Ashkenazi Jews, who were screened for Tay-Sachs disease, six were identified as Sandhoff carriers. Our data indicate that carrier detection requires measurement of both total and heat-stable enzyme activity.

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Year:  1978        PMID: 414620      PMCID: PMC1685463     

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


  22 in total

1.  Changes in human hexosaminidase isoenzyme distribution in body fluids during the course of tissue damage.

Authors:  S M Tucker; R G Price
Journal:  Biochem Soc Trans       Date:  1977       Impact factor: 5.407

2.  Letter: Screening for Tay-Sachs disease.

Authors: 
Journal:  Can Med Assoc J       Date:  1974-11-02       Impact factor: 8.262

3.  Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.

Authors:  H Galjaard; A Hoogeveen; H A de Wit-Verbeek; A J Reuser; W Keijzer; A Westerveld; D Bootsma
Journal:  Exp Cell Res       Date:  1974-08       Impact factor: 3.905

4.  A new variant of Sandhoff's disease.

Authors:  M W Spence; B A Ripley; J A Embil; J A Tibbles
Journal:  Pediatr Res       Date:  1974-06       Impact factor: 3.756

5.  Detection of GM2-gangliosidosis (Tay-Sachs and Sandhoff disease) gene carriers by serum hexosaminidase assay.

Authors:  B Molzer; H Bernheimer
Journal:  Clin Chim Acta       Date:  1976-11-15       Impact factor: 3.786

6.  Studies on human beta-D-N-acetylhexosaminidases. 3. Biochemical genetics of Tay-Sachs and Sandhoff's diseases.

Authors:  S K Srivastava; E Beutler
Journal:  J Biol Chem       Date:  1974-04-10       Impact factor: 5.157

7.  Hexosaminidase C in Tay-Sachs and Sandhoff disease.

Authors:  E Penton; L Poenaru; J C Dreyfus
Journal:  Biochim Biophys Acta       Date:  1975-05-23

8.  Juvenile Sandhoff disease: some properties of the residual hexosaminidase in cultured fibroblasts.

Authors:  S Wood; B G MacDougall
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

9.  Chemical characterization and subunit structure of human N-acetylhexosaminidases A and B.

Authors:  B Geiger; R Arnon
Journal:  Biochemistry       Date:  1976-08-10       Impact factor: 3.162

10.  Automated differentiation and measurement of hexosaminidase isoenzymes in biological fluids and its application to pre- and postnatal detection of Tay-Sachs disease.

Authors:  A Saifer; G W Parkhurst; J Amoroso
Journal:  Clin Chem       Date:  1975-03       Impact factor: 8.327

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  15 in total

Review 1.  Biochemistry and genetics of gangliosidoses.

Authors:  K Sandhoff; H Christomanou
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Authors:  C Bétard; A Rasquin-Weber; C Brewer; E Drouin; S Clark; A Verner; C Darmond-Zwaig; J Fortin; J Mercier; P Chagnon; T M Fujiwara; K Morgan; A Richter; T J Hudson; G A Mitchell
Journal:  Am J Hum Genet       Date:  2000-05-11       Impact factor: 11.025

3.  GM2 gangliosidoses: a review of cases confirmed by beta-N-acetylhexosaminidase assay.

Authors:  R Christopher; G R Rangaswamy; K T Shetty
Journal:  Indian J Pediatr       Date:  1995 Jul-Aug       Impact factor: 1.967

4.  Chromatofocusing coupled with automated assay for beta-hexosaminidase isoenzymes in GM2 gangliosidosis.

Authors:  A Orlacchio; C Maffei; C Emiliani; G V Coppa; L Felici
Journal:  Experientia       Date:  1985-04-15

5.  Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. II. Sandhoff disease gene frequencies in American Jewish and non-Jewish populations.

Authors:  R M Cantor; C Roy; J S Lim; M M Kaback
Journal:  Am J Hum Genet       Date:  1987-07       Impact factor: 11.025

6.  Evidence for a hybrid hexosaminidase isoenzyme in heterozygotes for Sandhoff disease.

Authors:  J A Lowden
Journal:  Am J Hum Genet       Date:  1979-05       Impact factor: 11.025

7.  Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. I. Statistical methods.

Authors:  R M Cantor; J S Lim; C Roy; M M Kaback
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

8.  Apparent hexosaminidase B deficiency in two healthy members of a pedigree.

Authors:  P Hechtman; A Rowlands
Journal:  Am J Hum Genet       Date:  1979-07       Impact factor: 11.025

9.  Incidence and carrier frequency of Sandhoff disease in Saskatchewan determined using a novel substrate with detection by tandem mass spectrometry and molecular genetic analysis.

Authors:  Braden Fitterer; Patricia Hall; Nick Antonishyn; Rajagopal Desikan; Michael Gelb; Denis Lehotay
Journal:  Mol Genet Metab       Date:  2014-01-13       Impact factor: 4.797

10.  Segregation of Tay-Sachs and Sandhoff alleles in a non-Jewish family.

Authors:  A B Lane; E Young; T Jenkins
Journal:  Am J Hum Genet       Date:  1980-11       Impact factor: 11.025

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