Results 61 to 70 of about 3,937 (169)
Human parvovirus infection and aplastic crisis in hereditary spherocytosis
Parvovirus B19 is usually associated with an acute, self-limiting disease. In patients with congenital haemolytic anaemia, infection with this virus can cause an aplastic crisis.
A Gogia +4 more
doaj
For hereditary spherocytosis complicated by cholelithiasis, cholecystectomy is simultaneously performed with splenectomy. However, jaundice promptly disappears after removing the spleen, and the risk for recurrent cholelithiasis decreases in majority of ...
Yutaka Yamada +7 more
doaj +1 more source
An overview of hereditary spherocytosis and the curative effects of splenectomy
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 ...
Kyril Turpaev +15 more
doaj +1 more source
A rare case of post-splenectomy gastric volvulus managed by laparoscopic anterior gastropexy
We report an extremely rare case of recurrent gastric volvulus after open splenectomy for hereditary spherocytosis. The initial episode was managed by endoscopic derotation.
Rahul Amreesh Gupta +2 more
doaj +1 more source
Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn
A term male newborn born to a mother who had hereditary spherocytosis presented with neonatal jaundice at 20 hours of life. Complete blood count showed hemoglobin 17.1 g/dL, MCV 104.2 fL, MCH 32.9 pg, and MCHC 31.6 g/dL.
Kanda Fanhchaksai +4 more
doaj +1 more source
Extramedullary paraspinal hematopoiesis in hereditary spherocytosis
Hereditary spherocytosis (HS) is a common inherited hemolytic anemia due to red cell membrane defects. Extramedullary hematopoiesis is a compensatory response to insufficient bone marrow blood cell production.
Gogia P, Goel R, Nayar S
doaj
Background Hereditary spherocytosis is the most common congenital anaemia in Europe. In patients with this disease, parvovirus B19 infection leads to aplastic crisis – a severe complication with significant morbidity and decrease in haemoglobin ...
Petr Birke +4 more
doaj +1 more source
Objective: The objective of this study was to pinpoint pathogenic genes and assess the mutagenic pathogenicity in two pediatric patients with hereditary spherocytosis.Methods: We utilized whole-exome sequencing (WES) for individual analysis (case 1) and ...
Ting Xiong +6 more
doaj +1 more source
Plenary Abstracts Session & Oral Presentations
HemaSphere, Volume 10, Issue S1, June 2026.
wiley +1 more source

