Beschreibung:
<jats:p>Variant AB of infantile G<jats:sub>M2</jats:sub> gangliosidosis is a fatal disease leading invariably to death within the first few years of life, due to the excessive storage of the glycolipids G<jats:sub>M2</jats:sub> and G<jats:sub>A2</jats:sub> which occurs in the nervous tissue of the patient. Unlike other variants of this hereditary disease, where a deficiency of hexosaminidase A, the ganglioside‐G<jats:sub>M2</jats:sub>‐degrading enzyme, could be demonstrated, the variant AB is characterized by a normal or even elevated level of this enzyme.</jats:p><jats:p>To examine the possibility of a mutant hexosaminidase A, well capable of hydrolyzing the fluorogenic synthetic substrates but unable to attack the ganglioside, the enzyme was isolated from a patient's tissue and characterized biochemically and immunologically in comparison with an enzyme preparation from normal control tissue. No differences between hexosaminidase A from normal and variant AB tissue could be detected indicating that the defect involved in this disease is not at the genetic level of production of either α or β chains of hexosaminidase A.</jats:p>