Results 1 to 10 of about 7,830 (207)

Hereditary Spherocytosis

open access: yesJournal of Lumbini Medical College, 2018
Introduction: Hereditary spherocytosis is a red cell membrane disorder that causes hemolytic anemia. Due to defective cell membrane, red cells are spherical shaped and result in their early lysis. Osmotic fragility of spherocytic red cell is increased.
Surendra Koju, Ramesh Makaju
doaj   +4 more sources

Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrin<sup>LELY</sup> in Trans. [PDF]

open access: yesAm J Hematol
American Journal of Hematology, Volume 100, Issue 12, Page 2355-2356, December 2025.
Molina-Arrebola MA, Bain BJ.
europepmc   +2 more sources

Post-splenectomy accessory spleen hyperfunction in children with hereditary spherocytosis: a rare case report and literature review [PDF]

open access: yesFrontiers in Pediatrics
ObjectiveTo 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

Hereditary spherocytosis

open access: yesMedical 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]

open access: yesJournal of Medical Case Reports
Background 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

Cerebrovascular involvement in hereditary spherocytosis: observational cohort and case-control MRI study [PDF]

open access: yesOrphanet Journal of Rare Diseases
Background 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

Cognitive impairment in hereditary spherocytosis. [PDF]

open access: yesBr J Haematol
British Journal of Haematology, Volume 207, Issue 4, Page 1719-1721, October 2025.
Tartaglione I   +12 more
europepmc   +2 more sources

Neonatal hereditary spherocytosis: a case report [PDF]

open access: yesItalian Journal of Pediatrics
Background 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

Pediatric splenectomy for hematologic disorders: two-decade experience and prophylactic cholecystectomy outcomes [PDF]

open access: yesBMC Surgery
Background 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

Hereditary Spherocytosis

open access: yesJournal of Associated Medical Sciences, 2015
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ละอองดาว สุวรรณชมภู   +1 more
doaj   +3 more sources

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