Results 41 to 50 of about 7,138 (202)

Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness

open access: yesThe Turkish Journal of Pediatrics, 2009
Thiamine-responsive megaloblastic anemia syndrome is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural hearing loss.
Hasan Onal   +7 more
doaj  

Effects of B9 and B12 vitamins deficiency on the genesis of megaloblastic anemia

open access: yesMedisur, 2023
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  

Bone Marrow Examination in Cases of Pancytopenia

open access: yesJournal of Nepal Medical Association, 2008
This study was carried to identify the causes of pancytopenia and to fi nd out the bone marrow morphology in cases of pancytopenia. It was a cross sectional study conducted over a period of two years in the Department of Pathology, Tribhuvan University ...
Abhimanyu Jha   +4 more
doaj   +1 more source

The effect of different types of anemia on HbA1c levels in non-diabetics

open access: yesBMC Endocrine Disorders, 2023
Background Diabetes mellitus is one of the most common diseases worldwide with significant morbidity and mortality. HbA1c remains one of the most important methods for diagnosis and monitoring of the disease.
Basil A. Alzahrani   +7 more
doaj   +1 more source

Concomitant use of metformin and proton pump inhibitors increases vitamin B12 deficiency risk in type 2 diabetes

open access: yesJournal of Diabetes Investigation, Volume 16, Issue 6, Page 1020-1027, June 2025.
The concomitant use of metformin and PPI was significantly associated with an increased risk of vitamin B12 deficiency in patients with type 2 diabetes. ABSTRACT Introduction Vitamin B12 deficiency is one of the adverse drug reactions of metformin and proton pump inhibitors (PPIs).
Choungwon Jung, Soyoung Park, Hyunah Kim
wiley   +1 more source

Impact of Metformin Therapy on Vitamin B12 Levels in Patients With Type 2 Diabetes Mellitus

open access: yesEndocrinology, Diabetes &Metabolism, Volume 8, Issue 3, May 2025.
The association between metformin treatment in type 2 DM and vitamin B12 deficiency. ABSTRACT Introduction Diabetes mellitus (DM) is a serious health condition affecting people worldwide with a high prevalence rate. DM is classified according to its aetiology into type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM); several risk factors
Sahar H. Mahmoud   +3 more
wiley   +1 more source

Rapid Improvement of Hyperpigmentation, Growth, and Developmental Milestones With High‐Dose Hydroxocobalamin, Betaine, and Folinic Acid Treatment: The First Patient With Cobalamin G Deficiency in Taiwan

open access: yesJIMD Reports, Volume 66, Issue 3, May 2025.
ABSTRACT In this report, we present the case of a 16‐month‐old patient who was diagnosed with cobalamin G deficiency at 4 months of age via whole exome sequencing by detecting compound heterozygous variants of uncertain significance (VUS) in the MTR gene: (1) c.1283T>A, p.Met428Lys; (2) c.2411T>C, p.Ile804Thr. Before the diagnosis, the initial clinical
Chi‐Tang Wu   +3 more
wiley   +1 more source

MEGALOBLASTIC ANEMIA AND PATTERN OF ITS PRESENTATION IN CHILDREN

open access: yesGomal Journal of Medical Sciences, 2016
Background: Megaloblastic anemia is common in clinical practice in children in Pakistan. Vitamin B12 and folate deficiency are the established causes. The aim of this study was to find the frequency of megaloblastic anemia, its clinical presentation and ...
Anwar Zeb Jan, Zahid Gul, Fahad Liaqat
doaj  

A Novel Mutation of SLC19A2 in a Chinese Zhuang Ethnic Family with Thiamine-Responsive Megaloblastic Anemia

open access: yesCellular Physiology and Biochemistry, 2018
Background/Aims: Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder resulting from mutations in SLC19A2, and is mainly characterized by megaloblastic anemia, diabetes, and progressive sensorineural hearing loss ...
Xiaoying Xian   +7 more
doaj   +1 more source

European Consensus on Malabsorption—UEG & SIGE, LGA, SPG, SRGH, CGS, ESPCG, EAGEN, ESPEN, and ESPGHAN. Part 1: Definitions, Clinical Phenotypes, and Diagnostic Testing for Malabsorption

open access: yesUnited European Gastroenterology Journal, Volume 13, Issue 4, Page 599-613, May 2025.
ABSTRACT Malabsorption is a complex and multifaceted condition characterised by the defective passage of nutrients into the blood and lymphatic streams. Several congenital or acquired disorders may cause either selective or global malabsorption in both children and adults, such as cystic fibrosis, exocrine pancreatic insufficiency (EPI), coeliac ...
Marco Vincenzo Lenti   +29 more
wiley   +1 more source

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