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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. 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 ...

  4. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    dominant Stargardt disease (macular degeneration) ABCA4, CNGB3, ELOVL4, PROM1: dominant or recessive 1-1.28:10,000 Stickler syndrome (multiple forms) COL11A1, COL11A2, COL2A1, COL9A1: dominant or recessive 1:7,500-9,000 (U.S.) Strudwick syndrome (spondyloepimetaphyseal dysplasia, Strudwick type) COL2A1: dominant TaySachs disease: HEXA (15 ...

  5. GM2 gangliosidoses - Wikipedia

    en.wikipedia.org/wiki/GM2_gangliosidoses

    TaySachs disease is a rare autosomal recessive genetic disorder that causes a progressive deterioration of nerve cells and of mental and physical abilities that begins around six months of age and usually results in death by the age of four. It is the most common of the GM2 gangliosidoses.

  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. 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.

  8. Chromosome 15 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_15

    Chromosome 15 is one of the 23 pairs of chromosomes in humans.People normally have two copies of this chromosome. Chromosome 15 spans about 99.7 million base pairs (the building material of DNA) and represents between 3% and 3.5% of the total DNA in cells.

  9. Dor Yeshorim - Wikipedia

    en.wikipedia.org/wiki/Dor_Yeshorim

    Rakow was a signatory to a subsequent letter stating that "Every individual has the privilege to perform the test in a manner consistent with his desires.” [14] In 2012, the Jewish Chronicle published a letter by a TaySachs carrier, who was hurt by a Dor Yeshorim organiser's insinuation that there was stigma attached to being a TaySachs ...