Results 51 to 60 of about 174,911 (201)

Morphological patterns of anemia among children aged 6 to 59 months attending Maputo Central Hospital, Maputo City Province, Mozambique

, 2023
Publisher Copyright: © (2023), (European Publishing). All Rights Reserved.Background and Objective: Globally, childhood anemia is a public health concern as it leads to poor health, physical and mental growth retardations, and increased risk of morbidity
Craveiro, Isabel, Cane, Réka Maulide, Keita, Youssouf, Varandas, Luís   +3 more
core   +1 more source

Evaluating the Efficacy of Cytokine‐Directed Therapies in the Management of VEXAS Syndrome

ACR Open Rheumatology, Volume 8, Issue 10, October 2026.
Objective To evaluate the efficacy of cytokine‐directed therapies in VEXAS (vacuoles, E1 enzyme, X‐linked, autoinflammatory somatic) syndrome using previously proposed treatment response criteria. Methods All patients with genetically confirmed VEXAS syndrome who received targeted therapies with JAK inhibitors (JAKi), tumor necrosis factor α inhibitors
Daniel Montes, Hannah E. Langenfeld, Andrew C. Hanson, Cynthia S. Crowson, Mrinal M. Patnaik, Ronald S. Go, Kambiz Kalantari, Yael Kusne, Terra Lasho, Abhishek A. Mangaonkar, Horatiu Olteanu, Kaaren K. Reichard, Megan M. Sullivan, David S. Viswanatha, Kenneth J. Warrington, Matthew J. Koster   +15 more
wiley   +1 more source

Bardet–Biedl Syndrome Presenting With Acute Kidney Injury Revealing Previously Undiagnosed Advanced Chronic Kidney Disease in a Young Adult: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Bardet–Biedl syndrome (BBS) is an autosomal recessive disorder characterized by obesity, rod‐cone dystrophy, polydactyly, developmental delay, renal dysfunction, and genitourinary abnormalities. We report the case of a 27‐year‐old female with previously undiagnosed BBS who presented with acute kidney injury precipitated by acute ...
Aqeel Abbas, Nouman Amjad, Amna Faheem Mufti, Muhammad Waqas, Minahil Iqbal, Hamza Ali, Amir Habib, Yahya Samadi, Muhammad Usman Haider   +8 more
wiley   +1 more source

Recurrent Projectile Vomiting as the Sole Presenting Feature of Coeliac Disease With Marsh–Oberhuber Grade 3C Enteropathy in a 13‐Year‐Old Girl: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT A 13‐year‐old girl presented with 4 months of recurrent projectile vomiting and weight loss without diarrhea. Investigations confirmed hypochloraemic metabolic alkalosis, strongly positive coeliac serology, nutritional deficiency, and biopsy‐proven Marsh–Oberhuber Grade 3C total villous atrophy.
Rahman Syed, Ameer Afzal Khan, Mehtab Alam, Suleman Shah, Mian Gul Rahman, Mohammed Al Meqbaali, Bilal Iqbal, Mohammed Al Sinani   +7 more
wiley   +1 more source

Basophilic Stippling Unmasks Pyrimidine 5′‐Nucleotidase Deficiency in a G6PD‐Deficient Patient

American Journal of Hematology, EarlyView.
Victor Bobée, Stéphane Moutereau, Maïssa Souissi, Pierre Lebreton, Loïc Garcon   +4 more
wiley   +1 more source

Hematological Indices Abnormalities Among Sudanese Children With Down Syndrome

Health Science Reports, Volume 9, Issue 10, October 2026.
ABSTRACT Background and Aims Down syndrome (DS) is a genetic condition caused by the triplication of chromosome 21. Currently, there is no available published data on hematological parameters among Sudanese children with Down syndrome. Therefore, this study aimed to investigate these parameters among this population.
Manasik Elghali, Abdelhakam G. Tamomh, Rooa Alhaj Ahmed, Tibyan Hassan Abdalmalik, Howida Hajhamd Ibrahim, Ibrahim K. Ibrahim   +5 more
wiley   +1 more source

X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation

, 2015
Macrocytic anemia with abnormal erythropoiesis is a common feature of megaloblastic anemias, congenital dyserythropoietic anemias, and myelodysplastic syndromes. Here, we characterized a family with multiple female individuals who have macrocytic anemia.
Ludwig, L.S., Ulirsch, J.C., Tchaikovskii, V., Shi, J., Wakabayashi, A., Lindsley, R.C., Bejar, R., Sankaran, V.G., Bishop, D.F., Lovitch, S.B., Steensma, D.P., Kadirvel, S.   +11 more
core   +1 more source

Macrocytic anemia induced via oral administration of toxic dose of acetaminophen

, 2022
The abuse of Acetaminophen (over-the-counter drug) is rapidly increasing globally, thus inducing physiological alterations and toxicity. In this study, it was hypothesized that overdose of acetaminophen may induce certain type of anemia; hence the type ...
Osah Martins Onwuka, Adaobi Linda Okerulu   +1 more
core   +1 more source

Atypical Presentation of UBE2T‐Related Fanconi Anemia With Immune‐Mediated Thrombocytopenia and Hematopoietic Somatic Mosaicism: A Case Report

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Fanconi anemia (FA) is a genetically heterogeneous disorder of chromosome instability leading to bone marrow failure (BMF) and other manifestations. We report a case of FA in which two atypical features initially obscured the diagnosis: the presence of T cell‐mediated thrombocytopenia, and somatic mosaicism leading to normal chromosome ...
Bridget T. Kiely, Alison A. Bertuch
wiley   +1 more source

Megaloblastic Anemia in a Patient with Addison’s Disease: A Case Report [PDF]

International Journal of Hematology-Oncology and Stem Cell Research, 2010
Primary 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. He  had been affected by a periodic paresthesia one month prior
Shahrbanou Keyhanian, Zahra Fotokian, Mohammad Mansour Saravi, Houman Ghoreyshi   +3 more
doaj   +1 more source