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Hereditary spherocytosis (HS) is a hereditary hemolytic ane-mia caused by the mutations in the genes encoding erythrocyte membrane proteins and is mostly inherited in an autosomal domi-nant manner.1- 3 HS is classified into four types according to the se-verity of the disease: trait, mild, moderate, and severe.
- Yangyang Wu, Lin Liao, Faquan Lin
- 2021
Oct 24, 2021 · PDF | Background Hereditary spherocytosis (HS), a commonly encountered hereditary hemolytic disease, is mostly inherited in an autosomal dominant... | Find, read and cite all the research you...
Hereditary spherocytosis (HS) is a heterogeneous group of disorders with regard to clinical severity, protein defects and mode of inheritance. It is relatively common in Caucasian populations; most affected individuals have mild or only moderate haemolysis.
Abstract. Background: Hereditary spherocytosis (HS), a commonly encountered hereditary hemolytic disease, is mostly inherited in an autosomal dominant manner. The clinical manifestations in patients with HS show obvious heterogeneity.
Nov 5, 2011 · Guidelines on hereditary spherocytosis (HS) published in 2004 (Bolton-Maggs et al, 2004) are here replaced to reflect changes in current opinion on the surgical management, (particularly the indications for concomitant splenectomy with cholecystectomy in children with mild HS, and concomitant cholecystectomy with splenectomy in those with
Feb 14, 2024 · Hereditary spherocytosis is a disorder in which the red blood cells are abnormal and fragile. Learn about the causes, symptoms, and treatment options for this disorder today.
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May 19, 2022 · Hereditary spherocytosis is a rare inherited disorder that requires lifelong medical care. Healthcare providers can treat the sometimes-serious medical conditions that hereditary spherocytosis causes.
