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Hereditary Heat-labile Hexosaminidase B: Its Implication for Recognizing Tay-Sachs Genotypes

Overview
Journal Am J Hum Genet
Publisher Cell Press
Specialty Genetics
Date 1981 Nov 1
PMID 6459736
Citations 3
Authors
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Abstract

Two pairs of alleles, at the two loci of hexosaminidase (HEX), were found to segregate in an Arab inbred family: the normal and the mutant Tay-Sachs (TSD) alleles of HEX A, and the normal and a mutant allele of HEX B. Since the mutant HEX B is heat labile, no reliable identification of TSD genotypes can be obtained in its presence, as long as the proportions of HEX A and B are estimated by the routinely used heat-inactivation method. The genotypes may be correctly identified in such cases by separation of the two isoenzymes on ion-exchange chromatography, estimating their individual activities, and calculating the ratio between them. Of the nine genotype combinations possible with these two pairs of alleles, five have been identified in the reported family by this procedure.

Citing Articles

Diagnosis and carrier detection of Tay-Sachs disease: direct determination of hexosaminidase A using 4-methylumbelliferyl derivatives of beta-N-acetylglucosamine-6-sulfate and beta-N-acetylgalactosamine-6-sulfate.

Reid J, Shapiro B, NADLER H Am J Hum Genet. 1985; 37(4):733-40.

PMID: 9556661 PMC: 1684631.


Thermal activation of hexosaminidase A in a genetic compound with Tay-Sachs disease.

Baylerian M, Momoi T, NADLER H J Inherit Metab Dis. 1983; 6(3):95-100.

PMID: 6230486 DOI: 10.1007/BF01800733.


Hereditary heat-labile hexosaminidase B: a variant whose homozygotes synthesize a functional HEX A.

Navon R, Kopel R, Nutman J, Frisch A, Conzelmann E, Sandhoff K Am J Hum Genet. 1985; 37(1):138-46.

PMID: 3156493 PMC: 1684534.

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