Advancing Hereditary Spherocytosis Care: New Technologies and Treatments
Hereditary spherocytosis (HS) is a genetic blood disorder characterized by abnormally shaped, spherical red blood cells (spherocytes). These fragile cells are prematurely destroyed, leading to anemia, jaundice, and splenomegaly. While HS has been recognized for decades, the landscape of its diagnosis and treatment is rapidly evolving in 2025. This blog post explores the emerging trends and...
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