Results 51 to 60 of about 156,004 (159)
Reversible Hyperpigmentation: A Diagnostic Dilemma
Vitamin B12 deficiency presents as megaloblastic anemia with neurological, skin and other clinical manifestations. We present here an interesting case of anemia presenting with generalized weakness and nonspecific symptoms in a female who is a vegetarian.
Somnath Maitra +2 more
doaj +1 more source
ABSTRACT A 70‐year‐old male with CLL presented with dengue fever complicated by AKI. A diagnostic challenge arose from overlapping features. Investigations showed leukocytosis, lymphocytosis, anemia, thrombocytopenia, positive Anti‐Dengue IgM, and renal impairment. Managed with supportive care, ibrutinib, and monitoring, with improvement.
Musawer Khan +8 more
wiley +1 more source
Role of myeloperoxidase index in differentiation of megaloblastic and aplastic anemia [PDF]
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
core +1 more source
ABSTRACT The orthostatic hypotension caused by vitamin B12 deficiency is extremely rare in young individuals. The serum vitamin B12 and anti‐intrinsic factor antibody levels of young patients with orthostatic hypotension should be evaluated regardless of the presence of anemia, and vitamin B12 administration should be promptly initiated.
Kenshin Tanaka +4 more
wiley +1 more source
Bilateral retinal hemorrhages from megaloblastic anemia: case report and review of literature
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 +3 more sources
Megaloblastic anemia due to anticonvulsant therapy [PDF]
Megaloblastic anemia is a well-recognized but rare complication of long term treatment with phenobarbitone, phenytoin and primidone. Evidence of megaloblastic haemopoiesis is commonly seen in patients undergoing anticonvulsant therapy.
Mangion, Pio
core
ABSTRACT Gaucher disease is a rare autosomal recessive lysosomal storage disorder that is caused by a deficiency of the enzyme “β‐glucocerebrosidase”, leading to the accumulation of glucocerebroside within macrophages. It commonly presents with hepatosplenomegaly, cytopenias, and bone marrow infiltration.
Muhammad Waqas +9 more
wiley +1 more source
Effects of B9 and B12 vitamins deficiency on the genesis of megaloblastic anemia
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
doaj
Imerslund‐Gräsbeck Syndrome Caused by Compound Heterozygous Mutations in the AMN Gene: A Case Report
ABSTRACT The 7‐year‐old girl had recurrent anemia for 6 years, showing large cell anemia. The parent‐derived AMN double heterozygous mutation was detected to confirm the diagnosis of IGS. The hemogram was normal after intramuscular injection of vitamin B12, and there were no other complications.
Cheng Chen +8 more
wiley +1 more source
Chia seed oil ameliorates obesity, dyslipidemia, and hepatorenal dysfunction in high‐fat diet–fed mice. ABSTRACT Chia seeds (Salvia hispanica L.) are recognized as a functional food with a nutrient‐dense profile and health‐promoting properties. In the present study, hexane‐extracted chia seed oil was investigated for anti‐obesity, hematoprotective, and
Sabbya Sachi +4 more
wiley +1 more source

