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  2. Amsterdam criteria - Wikipedia

    en.wikipedia.org/wiki/Amsterdam_criteria

    In 1997, the National Cancer Institute published a set of recommendations called the Bethesda guidelines for the identification of individuals who should receive genetic testing for Lynch syndrome related tumors. [6] The NCI revisited and revised these criteria in 2004. [7] The Revised Bethesda Guidelines are as follows:

  3. Hereditary nonpolyposis colorectal cancer - Wikipedia

    en.wikipedia.org/wiki/Hereditary_nonpolyposis...

    Hereditary nonpolyposis colorectal cancer (HNPCC) is a hereditary predisposition to colon cancer.. HNPCC includes (and was once synonymous with) [1] Lynch syndrome, an autosomal dominant genetic condition that is associated with a high risk of colon cancer, endometrial cancer (second most common), ovary, stomach, small intestine, hepatobiliary tract, upper urinary tract, brain, and skin. [2]

  4. Familial adenomatous polyposis - Wikipedia

    en.wikipedia.org/wiki/Familial_adenomatous_polyposis

    Three variants are known to exist, FAP and attenuated FAP (originally called hereditary flat adenoma syndrome [1]) are caused by APC gene defects on chromosome 5 while autosomal recessive FAP (or MUTYH-associated polyposis) is caused by defects in the MUTYH gene on chromosome 1. Of the three, FAP itself is the most severe and most common ...

  5. Microsatellite instability - Wikipedia

    en.wikipedia.org/wiki/Microsatellite_instability

    MSI-H status raises the possibility of Lynch syndrome, but MSI-H can also occur in patients without Lynch Syndrome and confirmation of Lynch Syndrome requires testing germline DNA. Lynch syndrome is associated with MSI and increases the risk for colon, endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and ...

  6. MUTYH-associated polyposis - Wikipedia

    en.wikipedia.org/wiki/MUTYH-associated_polyposis

    MUTYH-associated polyposis (also known as MYH-associated polyposis) is an autosomal recessive polyposis syndrome. [1] The disorder is caused by mutations in both alleles (genetic copies) of the DNA repair gene, MUTYH. The MUTYH gene encodes a base excision repair protein, which corrects oxidative damage to DNA.

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    mail.aol.com

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  8. Mismatch repair cancer syndrome - Wikipedia

    en.wikipedia.org/.../Mismatch_repair_cancer_syndrome

    Under the name constitutional mismatch repair-deficiency (CMMR-D), it has been mapped to MLH1, MSH2, MSH6 or PMS2. [2] Monoallelic mutations of these genes are observed in the condition known as Lynch syndrome or hereditary nonpolyposis colorectal cancer, while biallelic mutations are observed in CMMR-D. [3] People expressing the HNPCC (which itself is considered autosomal dominant) trait are ...

  9. Naomi Watts Mourns Longtime Collaborator David Lynch's Death ...

    www.aol.com/lifestyle/naomi-watts-mourns...

    Naomi Watts is mourning the loss of her Mulholland Drive director David Lynch.. The legendary filmmaker died at the age of 78, his family announced on Thursday, Jan. 16.. In a tribute on her ...