Results 1 to 10 of about 3,906 (147)

An overview of hereditary spherocytosis and the curative effects of splenectomy. [PDF]

Front Physiol
Hereditary 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 ...
Turpaev K, Bovt E, Shakhidzhanov S, Sinauridze E, Smetanina N, Koleva L, Kushnir N, Suvorova A, Ataullakhanov F.   +8 more
europepmc   +4 more sources

Transient Unexplained Severe Acute Hyperbilirubinaemia and Cholestasis in a Patient With Hereditary Spherocytosis. [PDF]

Case Reports Hepatol
Hereditary spherocytosis is an inherited red cell membrane disorder resulting in haemolytic anaemia. Recognised clinical manifestations include anaemia, jaundice, splenomegaly and gallstones.
Richardson J, Johnston M, Sefcick A, Oien K.   +3 more
europepmc   +2 more sources

Hereditary spherocytosis: Consequences of delayed diagnosis

SAGE Open Medicine, 2014
Objective: To determine whether patients with undiagnosed hereditary spherocytosis hospitalized for transfusions might have avoided hospitalization via earlier diagnosis. Study design: Charts of all (N = 30) patients with hereditary spherocytosis seen in
Allen R Chauvenet
exaly   +2 more sources

Hereditary spherocytosis

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. In severe cases, the disorder may present in early childhood, but in some cases it may go unnoticed until later in adult life.
Meenakshi Kalyan, Shubhangi A Kanitkar, Anu N Gaikwad, Harsh Kumar   +3 more
openaire   +3 more sources

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

Front Pediatr
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
He YF, Qi SQ, Bian J, Zhou CX, Zhang P.
europepmc   +2 more sources

Neonatal hereditary spherocytosis: a case report. [PDF]

Ital J Pediatr
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.
Coramusi C, Lucangeli N, Vadalà S, Parisi P, Scapillati ME.   +4 more
europepmc   +2 more sources

Hereditary spherocytosis

Eurasian Journal of Medicine, 2019
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Daniel Bell, Arlene Campos, Joshua Yap
doaj   +5 more sources

Is occlusive retinal vascular disease linked to hereditary spherocytosis postsplenectomy? A case series. [PDF]

J Med Case Rep
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.
Velcani F, Shah S, Zaugg BE, Teske MP, Batra NN.   +4 more
europepmc   +2 more sources

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

Orphanet J Rare Dis
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.
Manara R, Contieri M, Librizzi G, Palma T, Scianguetta S, Perna C, Villani AV, Matarese SMR, Luciano M, Amodio A, Pirozzi MA, Colombatti R, Santoro C, Cirillo M, Salle FD, Esposito F, Perrotta S, Tartaglione I.   +17 more
europepmc   +2 more sources

Hereditary Spherocytosis

Journal of Associated Medical Sciences, 2015
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ละอองดาว สุวรรณชมภู, Prasit Chanarat   +1 more
openaire   +2 more sources