Results 61 to 70 of about 3,937 (169)

Human parvovirus infection and aplastic crisis in hereditary spherocytosis

open access: yesCurrent Medicine Research and Practice, 2011
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  

Simultaneous gallbladder-preserving cholecystolithotomy and laparoscopic splenectomy as a surgical option for hereditary spherocytosis in a child: A case report

open access: yesJournal of Pediatric Surgery Case Reports, 2017
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

open access: yesFrontiers in Physiology
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

open access: yesJournal of Minimal Access Surgery, 2017
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

open access: yesCase Reports in Hematology, 2019
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

open access: yesAnnals of Thoracic Medicine, 2008
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  

Parvovirus B19-induced aplastic crises in children with hereditary spherocytosis in the Czech Republic: multicentre retrospective study

open access: yesBMC Infectious Diseases
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

Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis

open access: yesFrontiers in Genetics
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

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Poster Sessions

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

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