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It's All in the Blood - Hereditary Spherocytosis

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Manage episode 441459797 series 121255
Innhold levert av Medgeeks. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Medgeeks eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.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 episoder

Artwork
iconDel
 
Manage episode 441459797 series 121255
Innhold levert av Medgeeks. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Medgeeks eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.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 episoder

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