As a medical doctor and researcher, I am interested in rare congenital and genetic diseases and work to improve our knowledge and understanding of these disorders. I have a particular interest in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, a condition affecting one in 5,000 Danish women and involves the congenital absence of uterine development. My research integrates a range of disciplines, including clinical, laboratory, and epidemiological research.
My primary area of responsibility is genetic investigation and counseling of patients with genetic diseases. My research has a broad focus on mapping the causes of genetic diseases and improving our understanding of the natural history and epidemiology of these diseases.
