Results 21 to 30 of about 5,131 (199)
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
Hereditary spherocytosis: Retrospective evaluation of 65 children
The Turkish Journal of Pediatrics, 2018 Hereditary spherocytosis (HS) is a common cause of congenital hemolytic anemia in Caucasians and it could be diagnosed at any age. The aim of this study is to examine the demographic characteristics, clinical features and laboratory findings of children
Ali Güngör +5 more
doaj +3 more sources
Pediatric splenectomy for hematologic disorders: two-decade experience and prophylactic cholecystectomy outcomes [PDF]
BMC SurgeryBackground While splenectomy remains a cornerstone treatment for certain hematologic diseases, controversy persists regarding the optimal timing and indications for prophylactic cholecystectomy. This study evaluates long-term outcomes from a large single-
Oguzhan Uzaslan +4 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
Risk of hereditary spherocytosis misdiagnosis due to limited effective diagnostic methods
Revista Cubana de Medicina MilitarIntroduction: Hereditary spherocytosis is a prevalent congenital hemolytic erythrocyte membranopathy. Laboratory diagnosis is traditionally based on erythrocyte morphology, yet 20% of cases may lack visible spherocytes, leading to misdiagnosis.
Hien Thanh Dao +4 more
doaj +2 more sources
In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis. [PDF]
Br J HaematolSummary Hereditary spherocytosis (HS) is a hereditary haemolytic anaemia, caused by pathogenic variants in genes encoding red blood cell membrane proteins. Osmotic gradient ektacytometry evaluates red cell deformability and hydration and is increasingly used in the diagnosis of HS.
de Wilde JRA +9 more
europepmc +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
Hereditary Spherocytosis With Liver Transplantation After Cirrhosis: A Case Report
Frontiers in Medicine, 2022 The clinical manifestations of hereditary spherocytosis are similar to those of various hemolytic anemias, which causes hereditary spherocytosis to be difficult to diagnose clinically.
Xueliang Yang +6 more
doaj +1 more source