Tay-Sachs Disease, Volume 44

1st Edition

Serial Volume Editors: Robert Desnick Michael Kaback
Hardcover ISBN: 9780120176441
eBook ISBN: 9780080490304
Imprint: Academic Press
Published Date: 1st October 2001
Page Count: 363
161.00 + applicable tax
137.00 + applicable tax
110.00 + applicable tax
185.00 + applicable tax
Compatible Not compatible
VitalSource PC, Mac, iPhone & iPad Amazon Kindle eReader
ePub & PDF Apple & PC desktop. Mobile devices (Apple & Android) Amazon Kindle eReader
Mobi Amazon Kindle eReader Anything else

Institutional Access


Tay-Sachs disease is a rare hereditary disease caused by a genetic mutation that leaves the body unable to produce an enzyme necessary for fat metabolism in nerve cells, producing central nervous system degeneration. In infants, it is characterized by progressive mental deterioration, blindness, paralysis, epileptic seizures, and death by age four. Adult-onset Tay-Sachs occurs in persons who have a genetic mutation that is similar but allows some production of the missing enzyme. There is no treatment for Tay-Sachs. A test to determine whether an infant is carrying the Tay-Sachs disease was introduced in 1969. However, work continues to be done to help find a cure. Because there is no cure for this deadly disease, genetic research is essential.

Advances in Genetics presents an eclectic mix of articles of use to all human and molecular geneticists. They are written and edited by recognized leaders in the field and make this an essential series of books for anyone in the genetics field.


Pediatricians, geneticists, neurologists, and clinical biochemists


No. of pages:
© Academic Press 2001
Academic Press
eBook ISBN:
Hardcover ISBN:

About the Serial Volume Editors

Robert Desnick Serial Volume Editor

Affiliations and Expertise

Mout Sinai School of Medicine, New York, New York, U.S.A.

Michael Kaback Serial Volume Editor

Affiliations and Expertise

University of Califoria, San Diego, U.S.A.