Results 1 to 10 of about 312,696 (257)

Etiological study of microcytic hypochromic anemia

open access: yesJournal of Pathology of Nepal, 2016
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   +2 more sources

Relationship between Febrile Seizures and the Incidence of Microcytic Hypochromic Anemia in Children at Sanjiwani General Hospital, Gianyar, Indonesia

open access: yesBioscientia Medicina : Journal of Biomedicine and Translational Research, 2023
Background: Febrile seizures are the most common seizures in children. As many as 2% to 5% of children aged less than 5 years have had seizures accompanied by fever, and most occurrences are at the age of 17-23 months.
I. D. A. A. Diah Sutarini   +1 more
semanticscholar   +1 more source

Hemoglobin Variants in Patients With Microcytic Hypochromic Anemia: A Review of Indian Studies

open access: yesCureus, 2023
Microcytic hypochromic (MCHC) anemia with hemolytic components is common in clinical practice. Hemoglobinopathies and variants are one of the important underlying causes of MCHC anemia. The Indian population, by large, as various studies reported, showed
K. Kharche, A. Bhake
semanticscholar   +1 more source

Red cell distribution width’s role in differentiating iron deficiency anemia from other hypochromic microcytic anemias

open access: yesZanco Journal of Medical Sciences, 2021
Background and objective: The red cell distribution width is suggested to be a more sensitive indicator for microcytic hypochromic anemia. Therefore, this study aimed to determine the role of red cell distribution width in the diagnosis of iron ...
Shno Ibrahim Hussein   +1 more
doaj   +1 more source

Microcytic hypochromic Anemia is a risk factor for postoperative HAEC: A retrospective study

open access: yesFrontiers in Surgery, 2023
Background Hirschsprung-associated enterocolitis (HAEC) is a common and life-threatening complication of Hirschsprung's disease (HSCR), which can occur before and after surgery.
Yuanyuan Huang, Hongxia Ren
semanticscholar   +1 more source

A novel ENU-induced Cpox mutation causes microcytic hypochromic anemia in mice

open access: yesExperimental animals, 2022
Mouse models of red blood cell abnormalities are important for understanding the underlying molecular mechanisms of human erythrocytic diseases. DBA.B6-Mha (Microcytic hypochromic anemia) congenic mice were generated from the cross between N-ethyl-N ...
Y. Miyasaka   +5 more
semanticscholar   +1 more source

New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation

open access: yesInternational Journal of Molecular Sciences, 2022
Divalent metal-iron transporter 1 (DMT1) is a mammalian iron transporter encoded by the SLC11A2 gene. DMT1 has a vital role in iron homeostasis by mediating iron uptake in the intestine and kidneys and by recovering iron from recycling endosomes after ...
L. Romero-Cortadellas   +9 more
semanticscholar   +1 more source

Three-Month Iron Supplementation as Treatment for Microcytic Hypochromic Anemia in Pregnancy

open access: yesMajalah Kedokteran Bandung, 2021
In pregnant women there is a twofold increase in iron requirements due to increased blood volume without the expansion of plasma volume. Pregnant women are very prone to suffering from iron deficiency anemia.
Donel Donel   +3 more
doaj   +1 more source

CORRELATION BETWEEN THE PERCENTAGE OF HYPOCHROMIC ERYTHROCYTES AND FERRITINE LEVELS IN CHRONIC KIDNEY DISEASE PATIENTS UNDERGOING HEMODIALYSIS IN PKU BANTUL HOSPITAL

open access: yesBerkala Kedokteran, 2022
Abstrak: The incidence of CKD in the world is more than 500 million patients and up to 1.5 million patients need to undergo renal replacement therapy in the form of hemodialysis.
Seno Dwi Prasetyo   +2 more
doaj   +1 more source

Applications of Artificial Intelligence in Thalassemia: A Comprehensive Review

open access: yesDiagnostics, 2023
Thalassemia is an autosomal recessive genetic disorder that affects the beta or alpha subunits of the hemoglobin structure. Thalassemia is classified as a hypochromic microcytic anemia and a definitive diagnosis of thalassemia is made by genetic testing ...
Khaled Ferih   +7 more
doaj   +1 more source

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