Results 21 to 30 of about 8,383 (173)
Journal of Medical Case Reports, 2022 Background Hereditary folate malabsorption—a rare disorder caused by impairment of the folate transporter—can develop into severe folate deficiency manifesting as megaloblastic anemia and occasionally thrombocytopenia.
Yukari Sakurai +6 more
doaj +1 more source
Medical 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 +1 more source
Megaloblastic anemia in a teenage patient. [PDF]
Med J Armed Forces India, 2015 Mishra A +4 more
europepmc +3 more sources
Cochlear implant and thiamine-responsive megaloblastic anemia syndrome
Annals of Saudi Medicine, 2014 Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and bilateral sensorineural deafness, responding in varying degrees to thiamine treatment.
Abdulrahman Abdullah Hagr
doaj +1 more source
Evaluation of Thrombocytopenia in Megaloblastic Anemia by Platelet Indices and Megakaryocytes- Comparison with Hypoproduction and Hyperdestruction [PDF]
National Journal of Laboratory Medicine, 2017 Introduction: Thrombocytopenia may result from many mechanisms such as: marrow hypoplasia (decreased megakaryocytes), ineffective thrombopoiesis (normal to increased megakaryocytes) and increased destruction of platelets (increased megakaryocytes ...
Rajalakshmi Birur Rajashekar +2 more
doaj +1 more source
Pakistan Armed Forces Medical Journal, 2021 Objective: To study the diagnostic utility of lactate dehydrogenase levels in differentiating megaloblastic anemia from myelodysplastic anemia in Pakistan. Study Design: Comparative cross-sectional study.
Faraz Ali Rana +5 more
doaj
Thiamine-responsive megaloblastic anemia syndrome: A case report
Journal of Diabetology, 2020 Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare autosomal recessive disorder characterized by a cardinal triad consisting of megaloblastic anemia, sensorineural deafness, and diabetes mellitus.
Omkar Patil +5 more
doaj +1 more source
Two Cases of Primary Cold Agglutinin Disease Associated with Megaloblastic Anemia
Case 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 +1 more source
The 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 +1 more source
Journal of University College of Medicine and Dentistry, 2023 Objective: The study was performed to determine role of junk food intake in the development of megaloblastic anemia. Methodology: It was a clinical based cross-sectional study conducted at Mayo Hospital Lahore in collaboration with Pathology ...
Zunairah Mughal, Dr +5 more
doaj +1 more source