Results 1 to 10 of about 8,383 (173)

Massive Splenomegaly: A Rare Presentation of Megaloblastic Anemia [PDF]

open access: yesInternational Journal of Hematology-Oncology and Stem Cell Research, 2021
Megaloblastic anemia is a common disorder with various manifestations. Of the many causes, cobalamin or folate deficiency can eventuate into megaloblastic anemia.
Tahereh Gholipour   +4 more
doaj   +2 more sources

Megaloblastic anemia-related iron overload and erythroid regulators: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2021
Background In ineffective erythropoiesis, hepcidin synthesis is suppressed by erythroid regulators, namely erythroferrone and growth differentiation factor-15.
Nicolas Vallet   +10 more
doaj   +2 more sources

Megaloblastic Anemia in Bardet-Biedl Syndrome: A Rare Case Report [PDF]

open access: yesClinical Medicine Insights: Case Reports, 2023
Background: Bardet-Biedl syndrome (BBS) also known as Laurence-Moon-Bardet-Biedl syndrome one of the rarely reported genetic disorder characterized by an intellectual disability, limb, kidney abnormalities, obesity, and Rod-cone dystrophy.
Subtain Hassan   +8 more
doaj   +2 more sources

Severe megaloblastic anemia in a patient with advanced lung adenocarcinoma during treatment with erlotinib: a case report and literature review [PDF]

open access: yesBMC Pulmonary Medicine
Background Erlotinib is a first-generation, tyrosine kinase inhibitor of the epidermal growth factor receptor (EGFR-TKI) used for the treatment patients with NSCLC.
Xin Yan   +4 more
doaj   +2 more sources

Pulmonary embolism and megaloblastic anemia: is there a link? A case report an literature review [PDF]

open access: yesRadiology Case Reports, 2018
Many factors have been associated with venous thromboembolism. Among them, vitamin B12 deficiency can produce elevated homocysteine levels, which is a risk factor for venous embolism, since the latter interferes with the activation of Va coagulation ...
Grecia Iveth Raymundo-Martínez, MD   +6 more
doaj   +2 more sources

Novel Homozygous Variant in the SLC19A2 Gene Causing Thiamine Responsive Megaloblastic Anemia Syndrome: A Disease to Be Considered in Diabetes Clinics

open access: diamondEndocrinology Research and Practice
Thiamine-responsive megaloblastic anemia (TRMA) syndrome is a rare syndrome with an autosomal recessive manner that develops due to a mutation in the SLC19A2gene.
Burak Canvar Helvacı   +4 more
doaj   +2 more sources

An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment. [PDF]

open access: goldItal J Pediatr, 2023
Di Candia F   +13 more
europepmc   +3 more sources

Arrhythmia in thiamine responsive megaloblastic anemia syndrome [PDF]

open access: diamondThe 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   +2 more sources

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