Results 81 to 90 of about 8,233 (210)

Clinical characteristics of megaloblastic anemia with pancytopenia

Hematology
Objectives In this study, we aimed to explore the clinical characteristics of patients with megaloblastic anemia and pancytopenia.Methods Data on patient characteristics, laboratory examinations, clinical manifestations, and associated diseases were ...
Lin Tang, Jing Miao, Jinbi Wang
doaj   +1 more source

Bilateral retinal hemorrhages from megaloblastic anemia: case report and review of literature

, 1992
A 33-year-old woman who was a chronic alcohol abuser and had bilateral visual loss was found to have megaloblastic anemia with thrombocytopenia. Both fundi showed retinal venular dilatation and tortuosity, superficial and deep intraretinal hemorrhages ...
Lam, B L, Lam, S
core   +1 more source

Hypogammaglobulinemia in infantile megaloblastic anemia (Turkish)

, 1974
Three cases of infantile megaloblastic anemia are presented. All shared a common laboratory finding that total serum protein was near normal but gammaglobulin was very low. The relation between infection and gammaglobulin, ascorbic acid and folic acid is
Yalcin R.C., Ozgur S.
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Megaloblastic Anemia in a Patient with Addison’s Disease: A Case Report [PDF]

International Journal of Hematology-Oncology and Stem Cell Research, 2010
"nAbstract "nPrimary adrenal insufficiency (Addison’s disease) is due to adrenocortical disease. This study is about a 40 year old man who had been referred to a hematologist who assessed him for anemia.
Shahrbanou Keyhanian, Zahra Fotokian, Mohammad Mansour Saravi, Houman Ghoreyshi   +3 more
doaj  

Pancytopenia: A clinico-hematological study

Medical Journal of Dr. D.Y. Patil University, 2014
Background: A review of both Western and Indian literature shows that there are few comprehensive studies on pancytopenia. In India, the causes of pancytopenia are not well defined.
Fahim Manzoor, Manjiri N Karandikar, Ravindra C Nimbargi   +2 more
doaj   +1 more source

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report

, 2017
Background. Thiamine-responsive megaloblastic anemia syndrome (TRMA), also known as Rogers syndrome, is characterized by megaloblastic anemia, sensorineural hearing loss, and diabetes mellitus.
Koker, Sultan Aydin, Tunc, Selma, Ay, Yilmaz, Korkmaz, Huseyin A., Karapinar, Tuba H., Ozkan, Behzat, Demir, Korcan, Katipoglu, Nagehan, Oymak, Yesim, Vergin, Canan, Nalbantoglu, Ozlem, Yildiz, Melek, Hazan, Filiz   +12 more
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Rogers Syndrome, an Uncommon Cause of Megaloblastic Anemia: A Case Series

Advanced Biomedical Research
The present case series describes two male children of 5 months and 11 months old, having diabetes mellitus and megaloblastic anemia, but with no syndromic symptoms or organ involvement.
Reshma Roshan, Masarat Mehboob, Roman Latif, Javid R. Bhat, Santosh G. Rathod   +4 more
doaj   +1 more source

Thiamine-Responsive Megaloblastic Anemia Syndrome: Long Term Follow-Up

, 2009
Thiamine-responsive megaloblastic anemia is a rare autosomal recessive disorder whose main symptoms are anemia, diabetes mellitus, and sensorineural deafness.
BORGNA, Caterina, S. Pedretti, AZZALLI, Milena   +2 more
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Role of myeloperoxidase index in differentiation of megaloblastic and aplastic anemia

, 2004
BACKGROUND: Elevated neutrophil myeloperoxidase may have a role in the diagnosis of megaloblastic erythropoiesis. AIMS: To study the differentiating role of myeloperoxidase index in megaloblastic and aplastic anemia.
Dastgiri Saeed, Ziaei Jamal Eivazi
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Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source