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Journal 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. Case report: A 22 year old female presented with chief complain of abdominal pain. Initially she was
Ramesh Makaju, Surendra Koju
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Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis
Case Reports in Women's Health, 2017 Background: Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane.
Dawn M. Hannah +2 more
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Novel Variant of the SLC4A1 Gene Associated with Hereditary Spherocytosis
Biomedicines, 2023 Hereditary spherocytosis (HS) refers to the group of the most frequently occurring non-immune hereditary hemolytic anemia in people of Caucasian central or northern European ancestry.
Dżamila M. Bogusławska +5 more
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Spinal Cord Infarction in a Patient with Hereditary Spherocytosis: A Case Report and Discussion [PDF]
Case Reports in Neurological Medicine, 2016 The etiology of spinal cord infarcts (SCIs), besides being related to aortic perioperative events, in large subset of SCIs, remains cryptogenic.
Waqar Waheed +5 more
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Cholelitiasis in an adult patient with mild hereditary spherocytosis – a case report [PDF]
Archives of the Balkan Medical Union, 2018 Hereditary spherocytosis (HS) is an inherited abnormality of the red blood cell, caused by defects in structural membrane proteins. The condition is dominantly inherited in 75% of people.
Bogdan SOCEA +10 more
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Hematology, 2023 Background Severe autoimmune hemolytic anemia complicating hereditary spherocytosis is life threatening and has not been described in a case report. Here, we report a case in which this intractable disease was treated successfully with glucocorticoids ...
Na Wang +4 more
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Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis
Human Genome Variation, 2022 Blood disorder: Targeted sequencing helps diagnosis when symptoms vary Genetic testing can help accurately diagnose people suspected of having a rare blood disorder called hereditary spherocytosis, the clinical symptoms of which often vary.
Keiko Shimojima Yamamoto +9 more
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European Journal of Case Reports in Internal Medicine, 2021 Reactive thrombocytosis after splenectomy is a feared cause of thrombosis throughout the arterial and venous system. There are many causes of splenomegaly, ranging from cirrhosis to lymphoma to hereditary spherocytosis.
Chidinma Ejikeme +5 more
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Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis
Frontiers in Pediatrics, 2019 A 3-year-old girl was admitted to our hospital for the correction of atrial septal defect (ASD). Open heart operation with cardiopulmonary bypass is dangerous because the patient also had hereditary spherocytosis, which put her at risk for hemolytic ...
Zhixian Ji +6 more
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Hereditary Spherocytosis and Wandering Spleen
Pediatric Hematology and Oncology, 2013 Pelvic spleen is a very rare condition especially among children [1]. There were 130 pediatric cases reported in the literature [2].
Özgürler, Funda +4 more
openaire +6 more sources