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An overview of hereditary spherocytosis and the curative effects of splenectomy [PDF]
Frontiers in PhysiologyHereditary spherocytosis is a common hemolytic anemia with different severity. The causes of hereditary spherocytosis are mutations in genes that encode red blood cell (RBC) membrane and cytoskeletal proteins, including ankyrin-1, Band 3 (or AE1), α ...
Kyril Turpaev +15 more
exaly +4 more sources
Paediatrics and Child Health (United Kingdom), 2015 -
ละอองดาว สุวรรณชมภู +1 more
exaly +3 more sources
Transient Unexplained Severe Acute Hyperbilirubinaemia and Cholestasis in a Patient With Hereditary Spherocytosis [PDF]
Case Reports in HepatologyHereditary spherocytosis is an inherited red cell membrane disorder resulting in haemolytic anaemia. Recognised clinical manifestations include anaemia, jaundice, splenomegaly and gallstones.
Jennifer Richardson +3 more
doaj +2 more sources
Neonatal hereditary spherocytosis: a case report [PDF]
Italian Journal of PediatricsBackground Hereditary spherocytosis is a genetic disorder affecting red blood cell membranes, leading to increased destruction and haemolysis. In neonates, it ranges from asymptomatic to severe cases with anaemia, jaundice, and spleen issues.
Carolina Coramusi +4 more
doaj +2 more sources
Medical Journal of Dr. D.Y. Patil University, 2014 Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a fulminant hemolytic anemia.
Meenakshi Kalyan +3 more
doaj +2 more sources
Is occlusive retinal vascular disease linked to hereditary spherocytosis postsplenectomy? A case series [PDF]
Journal of Medical Case ReportsBackground To present two separate cases of occlusive retinal vascular disease with secondary cystoid macular edema in patients with a past medical history significant for hereditary spherocytosis and splenectomy.
Frida Velcani +4 more
doaj +2 more sources
Post-splenectomy accessory spleen hyperfunction in children with hereditary spherocytosis: a rare case report and literature review [PDF]
Frontiers in PediatricsObjectiveTo enhance the understanding of splenectomy in children with hereditary spherocytosis, specifically focusing on the preservation of accessory spleens or partial splenectomy.MethodsA retrospective review of clinical data and surgical methods of a
Yuan-fei He +4 more
doaj +2 more sources
Cerebrovascular involvement in hereditary spherocytosis: observational cohort and case-control MRI study [PDF]
Orphanet Journal of Rare DiseasesBackground Anecdotal Literature regarding hereditary spherocytosis, a rare hemolytic anemia, points to an early cerebrovascular involvement that would imply early strict patients’ monitoring and management.
Renzo Manara +17 more
doaj +2 more sources
A Case of Adrenal Myelolipoma Associated with Hereditary Spherocytosis
Clinical Pediatric Hematology-Oncology, 2021 Hereditary spherocytosis is the most common hereditary red blood cell membrane disorder. It results from a deficiency in certain proteins that are part of the red blood cell membrane cytoskeleton.
Dahui Gug +5 more
doaj +1 more source