Tay-Sachs DiseaseEdited by
- Robert Desnick, Mout Sinai School of Medicine, New York, New York, U.S.A.
- Michael Kaback, University of Califoria, San Diego, U.S.A.
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
Advances in Genetics
Hardbound, 363 Pages
Published: October 2001
Imprint: Academic Press