Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice
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DOI: 10.3892/mmr.2019.9947
Abstract: Hereditary spherocytosis (HS) is a common heterogeneous type of inherited hemolytic anemia characterized by jaundice and splenomegaly. Diagnosis of HS in neonates is considered unreliable, and is generally based on positive family history, spherocytes in… read more here.
Keywords: hemolytic jaundice; jaundice; hereditary spherocytosis; negative hemolytic ... See more keywords