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  2. GM2 gangliosidoses - Wikipedia

    en.wikipedia.org/wiki/GM2_gangliosidoses

    The diseases are better known by their individual names: TaySachs disease, AB variant, and Sandhoff disease. Beta-hexosaminidase is a vital hydrolytic enzyme, found in the lysosomes, that breaks down lipids. When beta-hexosaminidase is no longer functioning properly, the lipids accumulate in the nervous tissue of the brain and cause problems.

  3. 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 ...

  4. Lysosomal storage disease - Wikipedia

    en.wikipedia.org/wiki/Lysosomal_storage_disease

    TaySachs disease was the first of these disorders to be described, in 1881, followed by Gaucher disease in 1882. In the late 1950s and early 1960s, de Duve and colleagues, using cell fractionation techniques, cytological studies, and biochemical analyses, identified and characterized the lysosome as a cellular organelle responsible for ...

  5. 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 .

  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. Lysosome - Wikipedia

    en.wikipedia.org/wiki/Lysosome

    A lysosome (/ ˈ l aɪ s ə ˌ s oʊ m /) is a single membrane-bound organelle found in many animal cells. [1] [2] They are spherical vesicles that contain hydrolytic enzymes that digest many kinds of biomolecules. A lysosome has a specific composition, of both its membrane proteins and its lumenal proteins.

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  9. Category:Lysosomal storage diseases - Wikipedia

    en.wikipedia.org/wiki/Category:Lysosomal_storage...

    Lysosome; M. Mucolipidosis type IV; P. ... TaySachs disease This page was last edited on 25 July 2013, at 21:45 (UTC). Text is available under the Creative Commons ...