Results 41 to 50 of about 76,096 (261)

Follow-up, diagnosis, and outcomes of fever of unknown origin cases in whom no diagnosis was established after initial evaluation: an ID-IRI (Infectious Diseases - International Research Initiative) observational retrospective cohort study

BMC Infectious Diseases
Background/aim In fever of unknown origin (FUO), despite comprehensive evaluation a substantial proportion of patients may remain without a definitive diagnosis.
Umran Elbahr, Hakan Erdem, Amel Letaief, Svjetlana Grgić, Lysien Ivania Zambrano, Wissal Ben Yahia, Bilal Ahmad Rahimi, Magdalena Baymakova, Reham Khedr, Emmanuel Nsutebu, Gamze Şanlıdağ, Meliha Meriç Koç, Serkan Öncü, Kostadin Poposki, Gülden Eser-Karlıdağ, Oğuz Reşat Sipahi   +15 more
doaj   +1 more source

Pheochromocytoma presenting as fever of unknown origin, a case report

Case Reports, 2020
Introduction: Pheochromocytoma is a generally benign neoplasm derived from chromaffin cells of the adrenal medulla. It is characterized by the production of large amounts of catecholamines and also by the capacity to secrete bioactive peptides such as ...
Angélica María González-Clavijo, Juan David Muñoz-Loaiza, Jennifer Daniela Guzmán-Rojas, Johiner Jahir Vanegas-Antolinez, Laura Natalia Bermúdez-Silva, Luis Felipe Fierro-Maya   +5 more
doaj   +1 more source

Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley   +1 more source

A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita—Characterization Using Urine‐Derived Cells

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is defined as the presence of joint contractures affecting at least two body regions at birth. Three different ERGIC1 variants have been reported in individuals with AMC. Here, we report on a 16‐year‐old male with a homozygous ERGIC1 c.250+1G>A variant that was classified as a variant of uncertain ...
Lauren Kerr, Paul McKay, Juliana Marulanda, Zenghui Wu, Reggie Hamdy, Sena Tavukcu, Noémi Dahan‐Oliel, Frank Rauch   +7 more
wiley   +1 more source

Peripherally inserted central catheter line-induced fevers: a case report

Journal of Medical Case Reports
Background Peripherally inserted central catheter lines are increasingly common as medical innervation advances. Peripherally inserted central catheter lines are generally well tolerated with few complications, the most common being pain, bleeding, line ...
Catherine van’t Hoff, Benjamin H. L. Harris, Ahilan Kailaya-Vasan, Michael B. Fertleman, Louis J. Koizia   +4 more
doaj   +1 more source

Intra‐articular Orthobiologics Show Statistically but Not Clinically Meaningful Improvements Compared With Viscosupplementation in Knee Osteoarthritis: A Network Meta‐analysis of Randomized Controlled Trials

Arthroscopy, EarlyView.
Purpose To evaluate the comparative effectiveness of intra‐articular platelet‐rich plasma (PRP), stromal vascular fraction (SVF), bone marrow aspirate concentrate (BMAC), umbilical cord‐derived mesenchymal stem cell (UC‐MSC), and hyaluronic acid (HA) for pain relief and functional improvement in patients with knee osteoarthritis through network meta ...
Joo Hyung Han, Min Jung, Kwangho Chung, Hyun‐Soo Moon, Se‐Han Jung, Sung‐Hwan Kim   +5 more
wiley   +1 more source

A Common But Usually Overlooked Cause of Fever of Unknown Origin: Still’s Disease

Bagcilar Medical Bulletin, 2022
A wide variety of causes, ranging from bacterial or viral infections to malignancies, may be responsible from the development of fever of unknown origin (FUO).
Caner Varhan, İhsan Solmaz, Süleyman Özçaylak, Zeynep Kutlu, Elif Anık, Ahmet Engin Atay   +5 more
doaj   +1 more source

A Multifaceted Interplay Among Hemophagocytosis, Interleukin‐18, and Type I Interferon Distinguishes Still Disease From Other Autoinflammatory Diseases

Arthritis &Rheumatology, EarlyView.
Objective The unknown pathophysiology and the lack of specific features for systemic juvenile idiopathic arthritis and adult‐onset Still disease (collectively known as Still disease; SD) delay diagnosis and appropriate treatment. The goal of this study was to identify features and mechanisms that distinguish SD from other systemic autoinflammatory ...
Yvonne M. Mueller, Charlotte Girard, Harmen J. G. van de Werken, Stefan J. Erkeland, Dwin G. B. Grashof, Laurie Vaillant, Renske J. H. den Dekker, Iris van Zuijen, Sharon Veenbergen, Fanny Coffin, Eric Bindels, Yvan Jamilloux, Katerina Laskari, Vassili Soumelis, Bruno Fautrel, Cem Gabay, Peter D. Katsikis   +16 more
wiley   +1 more source

A PROSPECTIVE STUDY OF BRUCELLOSIS IN CHILDREN: RELATIVE FREQUENCY OF PANCYTOPENIA

Mediterranean Journal of Hematology and Infectious Diseases, 2013
Hematological complications in brucellosis are common. Pancytopenia, although mainly reported in adults has also been described in children with brucellosis.
Mohamed El Koumi, Mona Afify, Salha Al-Zahrani   +2 more
doaj   +1 more source

Inflammation Unchecked: Concurrent Kawasaki Disease and Stevens‐Johnson Syndrome in an 18‐Month‐Old Child

Arthritis Care &Research, EarlyView.
Catherine Deffendall, Jodi Backalar, Elizabeth Acevedo Zapata, Adriana Della Porta, Lorin Bibb, Tyler Reese, Charlotte M. Brown   +6 more
wiley   +1 more source