About Syeda Humaida Hasan
I am a pediatrician working in Bangladesh. Hard work is my passion, whether or not I directly benefit from it. I find satisfaction in the process itself and remain committed to it. My aim is to bridge clinical practice and research to improve the care of neonates and children. I am particularly interested in research on birth defects, child abandonment, and other public health issues affecting children.
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In our context, lack of consistent documentation makes it difficult to fully understand the true burden of birth defects. This realization, together with my early clinical experiences in neonatology, motivated me to explore this field more deeply, not only as a clinician but also as a researcher.
Recent Comments
Thank you for raising this important issue and for sharing such a personal and formative clinical experience.
This topic is also very close to my own professional path. My PhD research was devoted to the frequency of congenital anomalies among live births in Ukraine, and it served as a pilot study for the implementation of a Genetic Monitoring Programme. That programme no longer operates in its original form, but the work done during that period became part of a much longer and very difficult path toward systematic early detection of hereditary and congenital conditions.
In Ukraine, this path has taken almost two decades and has contributed to the development of neonatal screening and prenatal testing/diagnostic approaches aimed at earlier diagnosis, timely treatment, and prevention where possible. It was not a quick or simple process, and your post is an important reminder that behind every public health programme there are years of clinical observation, local data collection, advocacy, and persistence.
I fully agree that we still need stronger awareness, earlier diagnosis, better referral pathways, and more accessible specialized care for children with birth defects and their families.
Thank you very much for sharing your remarkable journey and for highlighting the long-term efforts required to establish a sustainable system for congenital anomaly surveillance and early diagnosis.
I look forward to exploring your work to gain knowledge and insights from the European experience in establishing genetic monitoring and birth defect surveillance systems. In Bangladesh, we are still far from developing a national birth defects registry; however, your experience provides valuable lessons and inspiration. I sincerely hope that, with sustained efforts in research, advocacy, and policy development, we will one day be able to establish such a system in our country.