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It's All in the Blood - Hereditary Spherocytosis

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Konten disediakan oleh Medgeeks. Semua konten podcast termasuk episode, grafik, dan deskripsi podcast diunggah dan disediakan langsung oleh Medgeeks atau mitra platform podcast mereka. Jika Anda yakin seseorang menggunakan karya berhak cipta Anda tanpa izin, Anda dapat mengikuti proses yang diuraikan di sini https://id.player.fm/legal.

In our upcoming hematology series, we'll delve into the fascinating world of genetic blood disorders. Our first episode will focus on Hereditary Spherocytosis (HS), a condition characterized by the production of abnormally shaped red blood cells resembling spheres instead of the usual disc-like shape.

We'll explore the underlying genetic mutation that causes HS and how it impacts the structure and function of red blood cells. Next, we'll discuss the common symptoms associated with HS, such as anemia, fatigue, jaundice, and abdominal pain. We'll also delve into the diagnostic process, including blood tests and genetic analysis.

Finally, we'll discuss the available treatment options for HS, which may include blood transfusions, medications, and in some cases, splenectomy.

Join Dr. Niket as we explore this rare genetic blood disorder and learn more about its impact on individuals and families.

September 9, 2024

  continue reading

410 episode

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iconBagikan
 
Manage episode 441459797 series 121255
Konten disediakan oleh Medgeeks. Semua konten podcast termasuk episode, grafik, dan deskripsi podcast diunggah dan disediakan langsung oleh Medgeeks atau mitra platform podcast mereka. Jika Anda yakin seseorang menggunakan karya berhak cipta Anda tanpa izin, Anda dapat mengikuti proses yang diuraikan di sini https://id.player.fm/legal.

In our upcoming hematology series, we'll delve into the fascinating world of genetic blood disorders. Our first episode will focus on Hereditary Spherocytosis (HS), a condition characterized by the production of abnormally shaped red blood cells resembling spheres instead of the usual disc-like shape.

We'll explore the underlying genetic mutation that causes HS and how it impacts the structure and function of red blood cells. Next, we'll discuss the common symptoms associated with HS, such as anemia, fatigue, jaundice, and abdominal pain. We'll also delve into the diagnostic process, including blood tests and genetic analysis.

Finally, we'll discuss the available treatment options for HS, which may include blood transfusions, medications, and in some cases, splenectomy.

Join Dr. Niket as we explore this rare genetic blood disorder and learn more about its impact on individuals and families.

September 9, 2024

  continue reading

410 episode

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