Results 21 to 30 of about 3,937 (169)
Spherocytic anemia in the newborn
The Turkish Journal of Pediatrics, 1962 A case is presented of hereditary spherocytosis diagnosed in a newborn infant who was found to be icteric on the first day of life. The establishment of the diagnosis is discussed, along with possible complications and therapy.
Roy E. Brown, E. Marvin Sokol
doaj +1 more source
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
Sarah C Steward +2 more
doaj +1 more source
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
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
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
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
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
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
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