Results 31 to 40 of about 7,830 (207)
Frontiers in Physiology, 2017 For many hereditary disorders, although the underlying genetic mutation may be known, the molecular mechanism leading to hemolytic anemia is still unclear and needs further investigation.
Laura Hertz +14 more
doaj +1 more source
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
doaj +1 more source
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
doaj +1 more source
Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis [PDF]
, 2005 Vertical and horizontal interactions between membrane constituents account for integrity, strength and deformability of the erythrocyte. Disruption of vertical interactions caused by membrane protein deficiencies in hereditary spherocytosis (HS), favor
Agre P +22 more
core +1 more source
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
doaj +1 more source
Spinal Cord Infarction in a Patient with Hereditary Spherocytosis: A Case Report and Discussion
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
doaj +1 more source
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
doaj +1 more source
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
doaj +1 more source
Analysis of Human Spleen Contamination [PDF]
, 2007 Besides carbon, oxygen and nitrogen, numerous other elements and their compounds are significant in the body of humans and other animals. Accumulation of some elements and their compounds is recognized by clinical and biochemical evaluation. The physical-
Jan Jakubovsky +2 more
core +2 more sources
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
doaj +1 more source