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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. Category:Autosomal recessive disorders - Wikipedia

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

    Batten disease; Behr syndrome; Berdon syndrome; Bernard–Soulier syndrome; Beta-ketothiolase deficiency; Beta-mannosidosis; Bietti's crystalline dystrophy; Biotin-thiamine-responsive basal ganglia disease; Biotinidase deficiency; Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome; Bloom syndrome; Blue diaper syndrome; Boucher ...

  5. Lipid storage disorder - Wikipedia

    en.wikipedia.org/wiki/Lipid_storage_disorder

    Many lipid storage disorders can be classified into the subgroup of sphingolipidoses, as they relate to sphingolipid metabolism. Members of this group include Niemann-Pick disease, Fabry disease, Krabbe disease, Gaucher disease, TaySachs disease, metachromatic leukodystrophy, multiple sulfatase deficiency, and Farber disease.

  6. 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 ...

  7. Medical genetics of Jews - Wikipedia

    en.wikipedia.org/wiki/Medical_genetics_of_Jews

    TaySachs disease, which can present as a fatal illness of children that causes mental deterioration prior to death, was historically extremely common among Ashkenazi Jews, [19] with lower levels of the disease in some Pennsylvania Dutch, Italian, Irish Catholic, and French Canadian descent, especially those living in the Cajun community of ...

  8. History of Tay–Sachs disease - Wikipedia

    en.wikipedia.org/wiki/History_of_TaySachs_disease

    David Slome, a researcher in the Department of Social Biology at the University of London, summarizing the knowledge of the time, concluded that TaySachs disease was caused by a single genetic defect, and that it followed an autosomal recessive pattern of inheritance. Slome also concluded that TaySachs was not exclusively a Jewish phenomenon.

  9. 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 ...