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 in h

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Raman and fourier transform infrared spectroscopy techniques for detection of coronavirus (COVID-19): a mini review

Coronavirus pandemic has been a huge jeopardy to human health in various systems since it outbroke, early detection and prevention of further escalation has become a priority.The current popular approach is to collect samples using the nasopharyngeal swab method and then test for RNA using Coffee Urns the real-time polymerase chain reaction, which

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