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Tay-Sachs Disease: Volume 44
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Tay-Sachs Disease: Volume 44 Hardcover - 2001 - 1st Edition

by Robert J. Desnick (Volume Editor); Michael M. Kaback (Volume Editor)


From the publisher

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.

First line

From the initial clinical descriptions of TSD at the end of the nineteenth century until the mid-1960s, major research contributions were predominantly in the areas of histopathology, lipid chemistry, genetic epidemiology, and ultrastructural analysis.

Details

  • Title Tay-Sachs Disease: Volume 44
  • Author Robert J. Desnick (Volume Editor); Michael M. Kaback (Volume Editor)
  • Binding Hardcover
  • Edition number 1st
  • Edition 1
  • Pages 363
  • Volumes 1
  • Language ENG
  • Publisher Academic Press, St Louis, Missouri, U.S.A.
  • Date 2001-10-01
  • ISBN 9780120176441 / 0120176440
  • Weight 1.36 lbs (0.62 kg)
  • Dimensions 9 x 6 x 0.88 in (22.86 x 15.24 x 2.24 cm)
  • Dewey Decimal Code 616
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Tay-Sachs Disease

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Tay-Sachs Disease (Volume 44) (Advances in Genetics, Volume 44)
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