Hereditary Spherocytosis (HS) comprises a diverse group of disorders characterized by the presence of spherocytes. Clinical manifestations may include anemia, jaundice, reticulocytosis, and splenomegaly. See results from a 45 year old female in our newsletter Heme Insights Issue 2.
► Back issues are available on the Heme Insights top page.
► Subscribe and receive the Heme Insights from the next issue: subscribe here.
