Gangliosidosis: A Brief Review Of Associated Neuropathology Essay

Gangliosidosis A Brief Review Of Associated NeuropathologyGangliosidosis is a lysosomal depot disease which affects primarily the nervous system. This disease is the result of an autosomal recessive allele genetic mutation which causes a lack or deficiency of an enzyme important in the metabolism of gangliosides. This deficient enzyme can vary depending on the type of mutation present causing either GM1 or GM2 gangliosidosis. Each of these will be discussed later, although the overall effects are similar. Increased amounts of gangliosides inside neurons leads to, of ten dollar bill lethal, neurodegenerative disorders. TAY- SACHS angiotensin-converting enzyme of the more common of these disorders is known as Tay--Sachs. Bernard Sachs was the commencement ceremony to get the cellular morphological features of this disease, distended cytoplasm of the neurons and ballooning of their dendrites. Later, in the 1930s, the term ganglioside was used to describe the accumulating material i n the neurons which was characteristic of the disease. infantile amaurotic idiocy is an infantile form of GM2 gangliosidosis close often found in Ashkenazi Jews. The rate of this disease is almost ten times higher in this population than in most former(a)s. Genetically, Tay-Sachs disease (TSD) is caused by a mutation at the alpha fractional monetary unit locus. In Ashkenazi Jews the mutation is primarily found in two forms. The first is a 4 base pair insertion into exon 11, the other is a G-to-C transversion mutation in the intron 12 splice site. A separate mutation has been found in the Maroc Jews, the deletion of a phenylalanine codon in the alpha subunit sequence. Recently, other mutations have been identified in these and other populations. In all cases, these mutations impair the alpha subunit of important hexosaminidase A resulting... ...8. Drucker, L.Identification and Rapid Detection of Three Tay--Sachs Mutations in the Moroccan Jew Population. Am. J. Human Genetics. 199 2 51 371-77. Fredrico, A. The Clinical Aspect of Adult Hexosaminidase Deficiencies. Developmental Neuroscience. 1991 13 280-287 Fukumizu, M. Tay-Sachs Disease Progression of Changes on Neuroimaging in Four Cases. Neuroradiology. 1992 34 483-486. Gravel, R.A. Biochemistry and Genetics of Tay-Sachs Disease. The Canadian Journal of Neurological Sciences. 1991 18 419-423. Maia, Maria. teen GM2 Variant B1 Clinical and Biochemical Study in Seven Patients. Neuropediatrics. 1990 21 18-23. Specola, N. The Juvenile and Chronic Forms of GM2 Gangliosidosis. Neurology. 1990 40 145-150. Suzuki, K. Neuropathology of Late Onset Gangliosidosis. Developmental Neuroscience. 199113 205-10.