A Case of Metformin-Related Megaloblastic Anemia Presenting with Palpitation [PDF]
Patient Safety and Quality Improvement Journal, 2015 Introduction:Metformin is the cornerstone of medical treatment in most diabetic patients with many beneficial effects on cardio-metabolic parameters.
Arash Gholoobi
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Effects of B9 and B12 vitamins deficiency on the genesis of megaloblastic anemia
Medisur, 2023 Megaloblastic anemia belongs to the subgroup of deficiency anemias. With the objective of describing the effect of B9 and B12 vitamins deficiency on the genesis of megaloblastic anemia, this research was carried out.
Karen Aracelly Tobar Armendariz +1 more
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The levels of nitric oxide in megaloblastic anemia
Turkish Journal of Hematology, 2009 Objective: The purpose of this study was to investigate the relationship between nitric oxide degradation products (nitrate and nitrite) levels and megaloblastic anemia which is treated with cyalocobalamin.
Emin Kaya +4 more
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Megaloblastic Anemia of Pregnancy: Characteristics of Pure Megaloblastic Anemia and Megaloblastic Anemia Associated with Iron Deficiency [PDF]
Blood, 1960 Abstract Morphology of the peripheral blood and bone marrow, iron, folic acid and vitamin B12 metabolism and estimation of erythrokinetics have been made in 17 patients with megaloblastic anemia of pregnancy. The peripheral blood showed the classic picture of megaloblastic anemia of pregnancy previously reported.
M, LAYRISSE +5 more
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Journal of Family Medicine and Primary Care, 2020 Vitamin B12 deficiency is seen in countries like India mainly because of predominantly vegetarian diet and is a significant health problem. Patients present with various neurological and hematological manifestations of megaloblastic anemia.
Kapil Bhalla +4 more
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Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia [PDF]
Disease and Diagnosis, 2022 Background: Autosomal recessive primary microcephaly-2 (MCPH2) is a rare genetic disorder with clinical and genetic heterogeneity. This study aimed to perform high-throughput whole-exome sequencing (WES) to facilitate the diagnosis of the genetic ...
Tahereh Dianat +3 more
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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
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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
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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
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To evaluate clinical spectrum of megaloblastic anemia in a tertiary care hospital central India
, 2022 Background: Megaloblastic anaemia is one of the frequently occurring diseases in a developing country such as India. Megaloblastic anemia occurs mainly because of vitamin B12 and folate deficiency.
Sharma, Ashish Kumar +2 more
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