Results 11 to 20 of about 8,391 (161)
Pediatric Rapunzel Syndrome Presenting With Jejunojejunal Intussusception Managed Surgically: A Rare Case Report. [PDF]
ABSTRACT Bezoars are masses of indigestible material within the gastrointestinal tract. Trichobezoars, composed of hair, are rare and typically occur in young females with psychiatric conditions. Rapunzel syndrome is a severe variant where the trichobezoar extends into the small intestine.
Irfan M +8 more
europepmc +2 more sources
AMA-Negative Primary Biliary Cholangitis and Autoimmune Hepatitis Overlap Syndrome Presenting With Bullous Pemphigoid: A Case Report. [PDF]
ABSTRACT Multiple autoimmune syndrome involves the concurrent presentation of at least three separate autoimmune conditions in one individual. When patients present with both autoimmune hepatitis (AIH) and primary biliary cholangitis (PBC) simultaneously, it is referred to as AIH‐PBC overlap syndrome.
Haque T +5 more
europepmc +2 more sources
Deep Vein Thrombosis in a Patient With Thalassemia Minor: A Case Report. [PDF]
ABSTRACT Deep vein thrombosis may develop in patients with beta‐thalassemia minor despite its benign hematologic course. Clinicians should consider thrombotic risk in these patients, ensuring timely recognition and management to prevent potentially life‐threatening complications.
Basnet A +3 more
europepmc +2 more sources
Correlation of automated cell counter RBC histograms and peripheral smear in anemia typing
Background: Red blood cell (RBC) indices and histogram obtained from automated hematology gives an idea about the morphological changes in anemia and therefore forms the fundamental process for diagnosis of anemia.
Hariom Meena +4 more
doaj +1 more source
Etiological study of microcytic hypochromic anemia
Background: Microcytic hypochromic anemia is a distinct morphologic subtype of anemia with well- de ned etiology and treatment. The objective of this study was to determine the etiology and frequency of microcytic hypochromic anemia.
S Kafle, M Lakhey
doaj +1 more source
Iron-refractory iron deficiency anemia (IRIDA) is an inherited iron metabolism disorder caused by mutations in TMPRSS6 gene encoding matriptase-2, which results in increased hepcidin synthesis.
Seda Çakmaklı +6 more
doaj +1 more source
Changes of hematological indices in patients with diffuse toxic goiter
Objective. To reveal the incidence of various morphological types and degrees of the anemia severity in patients with diffuse toxic goiter. Materials and methods.
F. H. Saidova +3 more
doaj +1 more source
Objective: The aim of this study was to evaluate the effectiveness of mature red cell and reticulocyte parameters to identify three conditions: iron deficiency anemia, anemia of chronic disease, and anemia of chronic disease associated with absolute iron
Ana Beatriz Barbosa Torino +4 more
doaj +1 more source
Background: World Health Organization recently acknowledged the proportion of anemia attributable to iron deficiency among under-five children could be lower than the previously assumed 50%.
Anteneh Omer +3 more
doaj +1 more source
Objective:The purpose of this study was to evaluate the effectiveness of mature red cell and reticulocyte parameters under three conditions: iron deficiency anemia, anemia of chronic disease, and anemia of chronic disease associated with absolute iron ...
Ana Beatriz Barbosa Torino +4 more
doaj +1 more source

