Results 11 to 20 of about 7,138 (202)

Megaloblastic anemia in a teenage patient. [PDF]

open access: yesMed J Armed Forces India, 2015
Retinal hemorrhages are usually seen in diabetic and/or hypertensive retinopathy, trauma, bleeding diathesis and with an increased intracranial pressure.1 Retinopathy due to megaloblastic anemia though rare, has been reported previously in literature.2 However Roth spots, in a case of megaloblastic anemia is considered very rare indeed.3, 4, 5 Finally ...
Mishra A   +4 more
europepmc   +5 more sources

Role of LDH levels in differentiating anemias

open access: yesAsian Journal of Medical Sciences, 2021
Background: There is a need to differentiate megaloblastic anemia from mixed deficiency anemia as both require different management protocols. With the acquisition of more information about them, tests such as serum vitamin estimation and Schilling test,
Noorin Zaidi   +4 more
doaj   +1 more source

MEGALOBLASTIC ANEMIA IN CHILDREN: CASE SERIES FROM A SINGLE INSTITUTION AND LITERATURE REVIEW [PDF]

open access: yesRomanian Journal of Pediatrics, 2018
Folic acid and cobalamin are B-group vitamins that play an essential role in many cellular processes. Deficiency in one or both of these vitamins causes megaloblastic anemia, a very rare anemia in children, which is characterized by the presence of ...
Andreea Oltean   +4 more
doaj   +1 more source

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   +1 more source

Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia [PDF]

open access: yesDisease 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
doaj   +1 more source

Idiopathic autoimmune hemolytic anemia along with concomitant vitamin B12 deficiency in an adolescent girl: A rare occurrence

open access: yesJournal 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
doaj   +1 more source

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