Article

Case Report: Concomitant Hereditary Spherocytosis and Protein C/Protein S Deficiency Presenting with Deep Vein Thrombosis

2026-08-25

Abstract excerpt

<title>Abstract</title> <p> <bold>Background</bold> Hereditary spherocytosis (HS) is an autosomal dominant haemolytic anaemia in which the erythrocyte’s membrane proteins are mutated. Clinical features of HS include haemolysis, anaemia. Splenomegaly, and jaundice. Protein C and S deficiency is also an autosomal dominant condition characterized by impaired inactivation of coagulation factors <italic>Va</italic>...

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Literature Corpus work: 11b4dd37-16fc-575a-927c-74d25fe34fdc
DOI: 10.21203/rs.3.rs-10638825/v1

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