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  2. HEXA - Wikipedia

    en.wikipedia.org/wiki/HEXA

    The HEXA gene is a protein encoding gene that codes for the lysosomal enzyme beta-hexosaminidase. This enzyme, combined with the GM2 activator protein, is responsible for the breakdown of ganglioside GM2 within the lysosome. Defects in the HEXA gene, however, prevent this degradation, leading to a buildup of toxins in brain and spinal cord cells.

  3. Tay–Sachs disease - Wikipedia

    en.wikipedia.org/wiki/Tay–Sachs_disease

    If a child received a normal copy from one parent and a mutated copy from the other, it is a carrier. [medical citation needed] Tay–Sachs results from mutations in the HEXA gene on chromosome 15, which encodes the alpha-subunit of beta-N-acetylhexosaminidase A, a lysosomal enzyme.

  4. Hexosaminidase - Wikipedia

    en.wikipedia.org/wiki/Hexosaminidase

    The most common mutation, which occurs in over 80 percent of Tay–Sachs 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. [12] Children born with Tay–Sachs usually die between two and four years of age from aspiration and ...

  5. Point mutation - Wikipedia

    en.wikipedia.org/wiki/Point_mutation

    The HEXA gene makes part of an enzyme called beta-hexosaminidase A, which plays a critical role in the nervous system. This enzyme helps break down a fatty substance called GM2 ganglioside in nerve cells. Mutations in the HEXA gene disrupt the activity of beta-hexosaminidase A, preventing the breakdown of the fatty substances.

  6. 29-Year-Old in ‘Catatonic State’ After Rare Disorder Causes ...

    www.aol.com/lifestyle/29-old-catatonic-state...

    Ben Tarver, 29, began having seizures and panic attacks in September before exhibiting symptoms of paranoia. By the middle of October, he was diagnosed with Anti-NMDA Receptor Encephalitis, a rare ...

  7. Frameshift mutation - Wikipedia

    en.wikipedia.org/wiki/Frameshift_mutation

    Mutations in the β-hexosaminidase A (Hex A) gene are known to affect the onset of Tay-Sachs, with 78 mutations of different types being described, 67 of which are known to cause disease. Most of the mutations observed (65/78) are single base substitutions or SNPs, 11 deletions, 1 large and 10 small, and 2 insertions. 8 of the observed ...

  8. Airbnb user fumes after company refuses to cancel booking ...

    www.aol.com/news/airbnb-user-fumes-company...

    An enraged traveler claims Airbnb is refusing to refund and rebook her after she attempted to cancel a vacation rental near the danger zone of the Los Angeles wildfires.. The rental firm has ...

  9. 'It doesn't make sense': Why millions of children have lost ...

    www.aol.com/doesnt-sense-why-millions-children...

    It’s been five months, and Isabella's parents say she still hasn’t gotten her Medicaid back even though her brother — same family, same income — never lost his.