Roles

ُُُُُEman Talha is one of the dedicated staff members at the Department of Histology and Medical Genetics at the College of Medicine, University of Tripoli. Since her appointment in 2011, she has made significant contributions to both the academic and research communities. With a focus on medical genetics and histology, she has been teaching several core subjects related to these fields, sharing her knowledge and expertise with both undergraduate and postgraduate students. Her teaching approach emphasizes the importance of problem-based learning, ensuring students can apply theoretical knowledge in practical and clinical scenarios.

In addition to her role as a lecturer, Eman Talha is actively involved in various research projects, particularly in the areas of genetic disorders and newborn screening programs. She has publication including studies on rare genetic conditions such as balanced reciprocal translocations and the ethical implications of these findings. Her research not only adds to the academic understanding of these issues but also contributes to the development of practical healthcare solutions in Libya. she has studies on congenetal adrenal hyperplasia and distribution of genetic diseases in Libya.

Eman is also Head of genetic department and a member of  the National  Newborn Screening  program and Rare Diseases  at the National Center for Disease Control in Libya. In this capacity, she oversees the implementation of screening programs aimed at early detection of genetic disorders in newborns, which is critical for providing timely interventions and improving patient outcomes. Her work in this area is highly regarded, and she regularly collaborates with national and international organizations to improve genetic healthcare services in the region.

Furthermore, Eman Talha is passionate about genetic counseling and frequently volunteers her expertise to help families navigate the complexities of genetic diagnoses and treatments. She is a member of the National Committee for Newborn Screening and Genetic Rare Diseases, where she helps shape policies and strategies that ensure comprehensive care for patients with rare conditions.

Fluent in both English and Arabic, Eman Talha is well-positioned to contribute to the global academic community, while also addressing the specific needs of the Libyan healthcare system. Her dedication to education, research, and patient care makes her a valuable asset to the University of Tripoli and the broader medical genetics field.

Careers

Lecturer at the Department of Histology and Medical Genetics, College of Medicine, University of Tripoli since 2011. Holds an MSc in Medical Genetics from the University of Glasgow and a diploma in Pediatric Medicine. Passionate about genetic counseling, medical genetics education, and research in rare diseases. Fluent in English and Arabic.م 

Research Interests

Eman Talha’s research focuses on the fields of medical genetics, rare diseases, and newborn screening programs. She is particularly interested in genetic counseling, histology, and the ethical implications of genetic conditions. Eman has contributed to research on balanced reciprocal translocations and is dedicated to advancing the understanding of genetics in the Libyan healthcare system. Additionally, she is actively involved in teaching medical genetics to undergraduate and postgraduate students, emphasizing problem-based learning approaches.

External Activities

Eman Talha is actively involved in advancing medical genetics education and providing genetic counseling services. She frequently delivers educational presentations on genetic counseling and screening programs to healthcare professionals, such as those held at Tripoli Medical Center and Tajora Hospital. Additionally, she volunteers as a genetic counselor, offering support and expertise to individuals and families facing genetic conditions. Eman is also a member of the National Committee for Newborn Screening and Rare Diseases, where she contributes to the development and implementation of national health programs.