The professor is also interested in other areas of clinical genetics: hereditary and congenital diseases, rare genetic syndromes, recurrent diseases within families, and the interpretation of genetic test results. He provides consultations regarding a potential hereditary predisposition to cancer, evaluates personal and family medical histories, and, when indicated, recommends targeted genetic testing. The results of these tests can help more accurately assess individual risk, develop a monitoring and early screening plan, and provide important information to the patient’s family members.
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