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  2. Tay–Sachs disease - Wikipedia

    en.wikipedia.org/wiki/TaySachs_disease

    TaySachs disease is inherited in an autosomal recessive pattern. The HEXA gene is located on the long (q) arm of human chromosome 15, between positions 23 and 24. TaySachs disease is an autosomal recessive genetic disorder, meaning that when both parents are carriers, there is a 25% risk of giving birth to an affected child with each ...

  3. GM2 gangliosidoses - Wikipedia

    en.wikipedia.org/wiki/GM2_gangliosidoses

    TaySachs disease has become famous as a public health model because an enzyme assay test for TSD was discovered and developed in the late 1960s and early 1970s, providing one of the first "mass screening" tools in medical genetics. It became a research and public health model for understanding and preventing all autosomal genetic disorders.

  4. Hexosaminidase - Wikipedia

    en.wikipedia.org/wiki/Hexosaminidase

    Over 100 different mutations have been discovered just in infantile cases of TaySachs disease alone. [11] The most common mutation, which occurs in over 80 percent of TaySachs patients, results from a four base pair addition (TATC) in exon 11 of the Hex A gene. This insertion leads to an early stop codon, which causes the Hex A deficiency ...

  5. GM1 gangliosidoses - Wikipedia

    en.wikipedia.org/wiki/GM1_gangliosidoses

    The GM1 gangliosidoses, usually shortened to GM1, are gangliosidoses caused by mutation in the GLB1 gene resulting in a deficiency of beta-galactosidase.The deficiency causes abnormal storage of acidic lipid materials in cells of the central and peripheral nervous systems, but particularly in the nerve cells, resulting in progressive neurodegeneration.

  6. Sphingolipidoses - Wikipedia

    en.wikipedia.org/wiki/Sphingolipidoses

    TaySachs disease: Hexosaminidase A: GM2 gangliosides in neurons: Neurodegeneration; Developmental disability; Early death; Autosomal recessive Approximately 1 in 320,000 newborns in the general population, [12] more in Ashkenazi Jews None Death by approx. 4 years for infantile TaySachs [13] Metachromatic leukodystrophy (MLD) Arylsulfatase ...

  7. Compound heterozygosity - Wikipedia

    en.wikipedia.org/wiki/Compound_heterozygosity

    TaySachs disease. In addition to its classic infantile form, Tay Sachs disease may present in juvenile or adult onset forms, often as the result of compound heterozygosity between two alleles, one that causes the classic infantile disease in homozygotes and another that allows some residual HEXA enzyme activity.

  8. Bitcoin's 2025 Outlook Suddenly Looks Uncertain: Here's Why - AOL

    www.aol.com/bitcoins-2025-outlook-suddenly-looks...

    The Federal Reserve's decision to remove its commitment to rate hikes in late January 2024 initially led to a strong rally. However, the lack of a clear timeline for rate cuts resulted in a six ...

  9. Health among the Amish - Wikipedia

    en.wikipedia.org/wiki/Health_among_the_Amish

    Tobacco-related cancers in Amish adults are 37 percent and non-tobacco-related cancers are 72 percent of the rate for Ohio adults. The Amish are protected against many types of cancer both through their lifestyle—there is very little tobacco or alcohol use and limited sexual partners—and through genes that may reduce their susceptibility to ...