Results 71 to 80 of about 6,451 (194)
ABSTRACT Background Non‐typeable Streptococcus pneumoniae (NT‐Sp) strains lack detectable capsules and are often missed by traditional serotyping. While associated primarily with asymptomatic carriage, NT‐Sp has emerged as a key player in antimicrobial resistance (AMR) gene dissemination and serotype replacement in the post‐vaccine era. This systematic
Robert K. Reeks +2 more
wiley +1 more source
Living Donor Liver Transplantation in Pediatric Situs Inversus: A Case Series and Systematic Review
ABSTRACT Liver transplantation (LT) in patients with situs inversus (S‐I) is rare and technically challenging. The literature on such cases, particularly in pediatric populations, remains limited. Here, we report the surgical considerations and outcomes of two pediatric recipients with situs inversus abdominalis who underwent liver transplantation for ...
Maria F. Fernandez +19 more
wiley +1 more source
Additional file 2: Fig. S1. Additional evidence for causative role of the de novo deletion 3p22.1. A—NGS results using IGV software showing homozygosity for all genetic variations found at locus. RPSA in patient with asplenia.
Sylwia Kołtan (8955506) +4 more
core +1 more source
A rare case of heme oxygenase deficiency: A case report and literature review
Key Clinical Message Heme oxygenase deficiency, a rare condition disrupting heme metabolism, has only nine reported cases. We present a 3‐year‐old boy with dysmorphic facies, asplenia, and normal bilirubin levels despite ongoing hemolysis.
Sai Santhosha Mrudula Alla +11 more
doaj +1 more source
We here report a case of Legionnaires’ disease in a splenectomised patient, complicated by rhabdomyolysis and acute renal failure and characterized by a poor clinical response to moxifloxacin.
Theocharis Koufakis +4 more
doaj +1 more source
Familial isolated congenital asplenia: case report and literature review.
Congenital asplenia is a rare life-threatening condition, often presenting with pneumococcal sepsis. It may arise as part of situs abnormalities or result from an unrelated specific defect of spleen development.
Stanley Zengeya +3 more
core +1 more source
A Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation
BACKGROUND Isolated congenital asplenia is a poorly understood and rare form of primary immunodeficiency, often associated with life-threatening infections. CASE REPORT We encountered a unique case of a 22-year-old asplenic male who presented with severe
Mazhar, Areej +3 more
core +1 more source
Infections are among the most common causes of morbidity and mortality in patients with hematological malignancies, and proper immunization can significantly reduce their incidence.
Iwona Hus +12 more
doaj +1 more source
Campylobacter jejuni bacteremia in a patient with asplenia and enteritis
Campylobacter bacteremia is an unusual presentation of a common infectious disease such as enteritis. We provide key teaching points about its presentation, risk factors, diagnosis and treatment.
Ramírez Isabel
doaj +1 more source
A fetal case of asplenia with fulminant pneumococcal infection [PDF]
We encountered a 14-month-old girl with asplenia who died of fulminant pneumococcal infection 2 hours after consultation. Inappropriate administration of an antibiotic for a few days prior to the onset of the episode may have been etiologically involved.
Shinohara, Tohru
core +1 more source

