THYROID CANCER IN A PATIENT WITH A GERMLINE MSH2 MUTATION. CASE REPORT AND REVIEW OF THE LYNCH SYNDROME EXPANDING TUMOUR SPECTRUM

Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum

Abstract Lynch syndrome (HNPCC) is a dominantly inherited disorder characterized by germline defects in DNA mismatch repair (MMR) genes and the development of a variety of cancers, predominantly colorectal and endometrial.We present a 44-year-old woman who was shown to carry the truncating MSH2 gene mutation that had previously been identified Fat

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Substantiation of technology for pates of milt from salmon fishes

Salmon milt is a valued raw material with high content of biologically active nucleoproteins, as DNA and RNA, and lipids enriched by phospholipids, sterols, fat-soluble vitamins, and polyene fatty acids, therefore development of new products on the base of fish milt with high nutritional value, caloric content and good organoleptic properties is ac

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