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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

    The disease results from mutations on chromosome 5 in the HEXB gene, critical for the lysosomal enzymes beta-N-acetylhexosaminidase A and B. Sandhoff disease is clinically indistinguishable from TaySachs disease. The most common form, infantile Sandhoff disease, is usually fatal by early childhood. [5]

  4. GM2-gangliosidosis, AB variant - Wikipedia

    en.wikipedia.org/wiki/GM2-gangliosidosis,_AB_variant

    Signs and symptoms of GM2-gangliosidosis, AB variant are identical with those of infantile TaySachs disease, except that enzyme assay testing shows normal levels of hexosaminidase A. [2] Infantile Sandhoff disease has similar symptoms and prognosis, except that there is deficiency of both hexosaminidase A and hexosaminidase B. Infants with this disorder typically appear normal until the age ...

  5. Compound heterozygosity - Wikipedia

    en.wikipedia.org/wiki/Compound_heterozygosity

    As molecular genomic techniques became available in the 1980s and 1990s, it became possible to explain a range of disorders in heterozygotes carrying one copy of one of the classic mutations for phenylketonuria. [5] TaySachs disease. In addition to its classic infantile form, Tay Sachs disease may present in juvenile or adult onset forms ...

  6. 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 ...

  7. 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.

  8. 7 Tips for Being More Confident With Your Body in 2025 - AOL

    www.aol.com/7-tips-being-more-confident...

    3. Celebrate Function, Not Just Form. Your body is more than a sculpture to be admired. It is the vehicle or vessel for your life and through which you may accomplish your dreams.

  9. Sphingolipidoses - Wikipedia

    en.wikipedia.org/wiki/Sphingolipidoses

    The main members of this group are Niemann–Pick disease, Fabry disease, Krabbe disease, Gaucher disease, TaySachs disease and metachromatic leukodystrophy. They are generally inherited in an autosomal recessive fashion, but notably Fabry disease is X-linked recessive .