Results 61 to 70 of about 48,173 (208)

Elusive Nexus: A Case of Megaloblastic Anaemia Secondary to Jejunal Diverticulosis [PDF]

Journal of Clinical and Diagnostic Research
Jejunal diverticulosis is a rare but often underdiagnosed condition that can lead to significant complications, including malabsorption and megaloblastic anaemia.
Gaurav A Chaudhary, Madhulika Mahashabde, Paidi Sai Krishna Reddy, Rishikesh S Chauhan, Jugal Sriram   +4 more
doaj   +1 more source

Megaloblastic Anaemia (MA)

Hematology, 2005
Megaloblastic Anaemia (MA) is caused by retarded purine and pyrimidine (notably thymidylate) synthesis. Therefore DNA does not replicate, but RNA and protein (including haemoglobin) synthesis continues leading to typical cell changes, especially in rapidly dividing tissues such as the bone marrow, testicles, gastrointestinal and bronchial epithelia ...
openaire   +2 more sources

Diagnostic Challenge of Pediatric Gaucher Disease in a Low‐Resource South Asian Setting: A Case Report

Clinical Case Reports, Volume 14, Issue 8, August 2026.
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, Rahila Bano, Muhammad Usman Haider, Kumar Abhishek, Arshad Mehmood, Aqeel Abbas, Abbas Ali, Talha Basheer, Rafiya Muhammad Altaf, Yahya Samadi   +9 more
wiley   +1 more source

Imerslund‐Gräsbeck Syndrome Caused by Compound Heterozygous Mutations in the AMN Gene: A Case Report

Clinical Case Reports, Volume 14, Issue 8, August 2026.
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, Yijia Min, Xiaoping Ye, Yu Ma, Huiqing Ge, Jingying Chou, Xiaoling Yang, Yingying Cui, Xiaochun Zhang   +8 more
wiley   +1 more source

A Study on Megaloblastic Anaemia and Pancytopenia

, 2019
Background: Megaloblastic Anaemia and pancytopenia are common medical problems, Vitamin B12and folic acid deficiencies are common  causes for megaloblastic Anaemia.
Reddy, P Sashikanth, Srinivas, S
core  

Utility of serum lactate dehydrogenase in the diagnosis of megaloblastic anemia [PDF]

, 2018
Background: Megaloblastc anemia corresponds to severe macrocytic anemia with hypersegmented neutrophils and very high serum Lactate Dehydrogenase (LDH). The present study was undertaken to evaluate the utility of serum LDH and chloroform inhibited serum ...
Jadhav, D. S., Gaikwad, Amrapali L.
core   +1 more source

Dose‐Dependent Anti‐Obesity and Protective Effects of Chia (Salvia hispanica L.) Seed Oil Against Hematological and Hepatorenal Dysfunction in High‐Fat Diet–Fed Mice

Food Science &Nutrition, Volume 14, Issue 8, August 2026.
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, Mst. Prianka Jahan, Sree Alok Kumar, Mahmudul Hasan Sikder, Md. Zahorul Islam   +4 more
wiley   +1 more source

Phenytoin Intake in Mothers Resulting in Early Onset Infantile Tremor Syndrome in Children: A Report of Two Cases [PDF]

Journal of Clinical and Diagnostic Research
Infantile Tremor Syndrome (ITS) is a complex neurological syndrome that affects exclusively breastfed infants, typically seen between 9 to 12 months of age.
Payal Mittal, Rohan Acharya, Dinkar Yadav, Kapil Bhalla, Shuchi Bhalla   +4 more
doaj   +1 more source

Identification of transcobalamin deficiency with two novel mutations in the TCN2 gene in a Chinese girl with abnormal immunity: a case report

BMC Pediatrics, 2020
Background Transcobalamin (TC) transports vitamin B12 from blood into cells. TC II deficiency is a rare autosomal recessive disorder. It is characterized by failure to thrive, diarrhoea, pallor, anaemia, pancytopenia or agammaglobulinemia.
Shihong Zhan, Fangfang Cheng, Hailong He, Shaoyan Hu, Xing Feng   +4 more
doaj   +1 more source

Elevated Hemoglobin A2: A Molecular Revisited, and Implications to β‐Thalassemia Screening

Journal of Clinical Laboratory Analysis, Volume 40, Issue 15, August 2026.
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, Anupong Pansuwan, Hataichanok Srivorakun, Attawut Chaibunruang, Supawadee Yamsri, Wanicha Tepakhan, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen   +8 more
wiley   +1 more source