Results 11 to 20 of about 8,214 (184)

Megaloblastic anemia associated with small bowel resection in an adult patient

open access: yesNigerian Journal of Medicine, 2021
Megaloblastic anemia is characterized by macro-ovalocytosis, cytopenias, and nucleocytoplasmic maturation asynchrony of marrow erythroblast. The development of megaloblastic anemia is usually insidious in onset, and symptoms are present only in severely ...
Ajayi Adeleke Ibijola   +1 more
doaj   +3 more sources

Megaloblastic anemia - A clinical spectrum and a hematological profile: The day-to-day public health problem

open access: yesMedical Journal of Dr. D.Y. Patil University, 2016
Aims and Objectives: To know the various parameters and diagnostic approach of megaloblastic anemia. To know the age incidence and sex ratio. Materials and Methods: A hospital-based retrospective and prospective study was done for a period of 1-year ...
S Srikanth
doaj   +2 more sources

Megaloblastic anemia in Japan.

open access: yesActa medica Okayama, 1978
Since 1903, 744 cases of megaloblastic anemia have been reported in Japan: 490 cases of pernicious anemia; 95 cases associated with pregnancy; 66 cases after gastrectomy; 22 cases of megaloblastic anemia of infants; 21 cases of folic acid deficiency other than pregnancy and 19 cases of vitamin B12 malabsorption after ileal resection.
Taguchi, Hirokuni
openaire   +4 more sources

Evaluation of Clinical Profile and Hematological Parameters of Cases of Megaloblastic Anemia

open access: yesNational Journal of Community Medicine, 2017
Background: Megaloblastic anemia is not uncommon in India. In India, the most common cause of megaloblastic anemia is nutritional where as it is the pernicious anemia in Northern Europe. Aims and objectives: To study age and gender-wise distribution,
Hemang N Suthar, Tejas N Shah
doaj   +1 more source

Two Cases of Primary Cold Agglutinin Disease Associated with Megaloblastic Anemia

open access: yesCase Reports in Hematology, 2015
We report two cases of primary cold agglutinin disease (CAD) associated with megaloblastic anemia in Japanese elderly patients. Case 1 was a 67-year-old male and Case 2 was a 55-year-old male.
Shinsaku Imashuku   +3 more
doaj   +2 more sources

Iron deficiency anemia and megaloblastic anemia in obese patients

open access: yesRomanian Journal of Internal Medicine, 2017
Background. The association between obesity and different types of anemia remained uncertain. The present study aimed to assess the relation between obesity parameters and the occurrence of iron deficiency anemia and also megaloblastic anemia among ...
Arshad Mahmoud   +5 more
doaj   +2 more sources

Thiamine– Responsive Megaloblastic Anemia Syndrome

open access: yesMajallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2009
Thiamine Responsive megaloblastic anemia in DIDMOA (Wolfram) syndrome has an autosomal- recessive mode of inheritance . Megaloblastic anemia and sideroblastic anemia is accompanied by diabetes insipidus (DI), diabetes mellitus (DM) ,optic atrophy (OA ...
F Motavaselian   +5 more
doaj   +1 more source

Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness

open access: yesThe Turkish Journal of Pediatrics, 2009
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural hearing loss.
Hasan Onal   +7 more
doaj   +3 more sources

A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome

open access: yesThe Turkish Journal of Pediatrics, 2019
Thiamine-responsive megaloblastic anemia (TRMA) is a very rare syndrome characterized by the triad of early onset megaloblastic anemia, sensorineural deafness and diabetes mellitus.
Işık Odaman-Al   +8 more
doaj   +3 more sources

Arrhythmia in thiamine responsive megaloblastic anemia syndrome

open access: yesThe Turkish Journal of Pediatrics, 2018
Thiamine responsive megaloblastic anemia syndrome (TRMAS) is a rare, autosomal recessive disorder characterized by megaloblastic anemia, diabetes mellitus, and progressive sensorineural deafness.
Mustafa Argun   +6 more
doaj   +3 more sources

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