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Article Synopsis
  • - Ovarian cancer often goes undetected until advanced stages due to vague symptoms and is linked to genetic mutations, particularly in BRCA1 and BRCA2 genes associated with family history.
  • - A study on 30 women with confirmed ovarian cancer found multiple genetic variants, including some novel ones, but did not identify the known BRCA founder mutations in the participants.
  • - While BRCA mutations account for a significant portion of familial ovarian cancer cases, they only explain a fraction of the overall genetic risk, suggesting the involvement of other genetic factors like single nucleotide polymorphisms (SNPs).
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