Results 51 to 60 of about 45,554 (205)
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
Spectrum of Pancytopenia in Local Population
Objective: To determine the frequency of pancytopenia aetiologies in local population. Study Design: Cross sectional study Place and Duration of Study: Haematology Department, Armed Forces Institute of Pathology, Rawalpindi Pakistan, from Jun 2020 ...
Syeda Samia Shafaat +3 more
doaj +1 more source
A Study of Bone Marrow Examination in Cases of Pancytopenia [PDF]
Bone marrow examination (aspiration and biopsy) carried out in 30 cases having pancytopenia, had megaloblastic anemia as the commonest cause (46.6%) of pancytopenia.
Manjula P. Biradar +2 more
doaj
Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm
Background Proteinuria is a common clinical presentation, the diagnostic workup for which involves many non-invasive and invasive investigations. We report on two siblings that highlight the clinically relevant functional role of cubulin for albumin ...
Kushani Jayasinghe +8 more
doaj +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
Megaloblastic anaemia, diabetes and deafness in a 2-year-old child [PDF]
Megaloblastic anaemia in childhood usually occurs as a result of dietary folate deficiency or, rarely, congenital disorders of vitamin B12 metabolism. We present a 2-year-old girl with megaloblastic anaemia and insulin-dependent diabetes mellitus, both ...
Hartley, Patricia S +3 more
core
Anaemia in Pregnancy and Infant Mortality in Tanzania. [PDF]
Tanzania is an area of moderate to high risk for severe anaemia during pregnancy. There is extensive literature examining the consequences of severe anaemia for pregnant women, but the impact this problem has on their infants in malaria-endemic regions ...
Mukasa, Oscar +13 more
core +1 more source
Vitamin B12 deficiency is common in developing countries and should be suspected in patients with unexplained anaemia or neurological symptoms. Dermatological manifestations associated with this deficiency include skin hyper- or hypopigmentation, angular
Kawther El-Shafie +6 more
doaj +3 more sources
Elevated Hemoglobin A2: A Molecular Revisited, and Implications to β‐Thalassemia Screening
In Thailand, the Hb A2 cut‐off value for β‐thalassemia carrier has been changed from 4.0% to 3.6% since 2015. We examined the molecular basis of β‐thalassemia in a large cohort of Thai subjects with this change. The molecular basis of β‐thalassemia was updated, and a change in the Hb A2 cut‐off can alter this spectrum.
Kritsada Singha +8 more
wiley +1 more source
Elusive Nexus: A Case of Megaloblastic Anaemia Secondary to Jejunal Diverticulosis [PDF]
Jejunal diverticulosis is a rare but often underdiagnosed condition that can lead to significant complications, including malabsorption and megaloblastic anaemia.
Gaurav A Chaudhary +4 more
doaj +1 more source

