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Episode 092: Heme Consult Series: Congenital Causes of Hemolytic Anemia

The Fellow on Call: The Heme/Onc Podcast

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Diagnosis and Treatment of Hereditary Membrane Disorders

The chapter delves into identifying membrane disorders in patients with chronic asymptomatic anemia and low hemolysis levels, focusing on hereditary spherocytosis and hereditary elliptocytosis. It covers the prevalence, genetic mutations, hemolysis mechanism, lab findings, and treatment considerations for these conditions, emphasizing the importance of peripheral smear examination and functional tests for definitive diagnosis.

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