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  2. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    Specialty. Medical genetics. Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. [1] The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18. [2]

  3. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Proximal 18q-is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. This deletion involves the proximal (near the centromere ) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [1]

  4. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    1 per 5,000 births [3] Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [3] Many parts of the body are affected. [3] Babies are often born small and have heart defects. [3] Other features include a small head, small jaw, clenched fists with overlapping ...

  5. Chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_18

    Chromosome 18 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of DNA ) and represents about 2.5 percent of the total DNA in cells .

  6. New criteria defined for memory loss condition often mistaken ...

    www.aol.com/criteria-defined-memory-loss...

    Now, scientists from the Mayo Clinic have identified another memory-loss condition found in older adults that is frequently misdiagnosed as Alzheimer’s disease. Researchers have developed new ...

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    C – Whole chromosome extra, missing, or both (see chromosome abnormality) T – Trinucleotide repeat disorders: gene is extended in length. A cherry red spot, which can be a feature of several storage disorders, including Tay–Sachs disease. Disorder. Chromosome. Mutation. Angelman syndrome. 15q. DCP.

  8. Healthy diet may lower glucose levels, cut diabetes risk ...

    www.aol.com/lifestyle/healthy-diet-may-lower...

    A new study found that a healthy diet may produce lower blood glucose levels and reduce the risk of type 2 diabetes in men regardless of any genetic predisposition to the condition. The study ...

  9. Birth defect - Wikipedia

    en.wikipedia.org/wiki/Birth_defect

    A birth defect, also known as a congenital disorder, is an abnormal condition that is present at birth regardless of its cause. [2] Birth defects may result in disabilities that may be physical, intellectual, or developmental. [2] The disabilities can range from mild to severe. [6]