Results 31 to 40 of about 12,922 (226)

Management of Spontaneous Crystalline Lens Luxation in a Patient Diagnosed with Takayasu’s Disease

Diagnostics, 2023
Takayasu’s disease is a chronic granulomatous arteriopathy that affects large vessels and their major branches. Nonspecific symptoms characterize the early phase, whereas findings of arterial occlusion and aneurysmal formation become manifest later ...
Elvia Mastrogiuseppe, Maria Pia Pirraglia, Lorenzo Sampalmieri, Ludovico Iannetti, Alessandro Beccia, Magda Gharbiya   +5 more
doaj   +1 more source

Takayasu arteritis a cause of hypertensive disorder of pregnancy: a case report

Journal of Medical Case Reports, 2018
Background Takayasu arteritis is a rare, chronic, granulomatous systemic vasculitis of unknown etiology and a few cases have been reported in pregnancy. In pregnancies concomitant with Takayasu arteritis or after diagnosis, Takayasu arteritis negatively ...
Jesus Lumbreras-Marquez, Roberto Arturo Castillo-Reyther, Salvador De-la-Maza-Labastida, Fernando Vazquez-Alaniz   +3 more
doaj   +1 more source

Abnormal molecular response to Takayasu arteritis causing extensive large-vessel calcification

Journal of Vascular Surgery Cases and Innovative Techniques, 2016
Takayasu arteritis is a large-vessel vasculitis that often results in pulselessness due to fibrotic stenoses. Whereas minor calcification is sometimes seen with Takayasu arteritis, it rarely causes stenosis.
Brandon T. Garland, MD, Manfred Boehm, MD, Peter C. Grayson, MD, Cynthia St Hilaire, PhD, Alessandra Brofferio, MD, Benjamin W. Starnes, MD   +5 more
doaj   +1 more source

Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT RASopathies are clinically overlapping neurodevelopmental syndromes resulting from germline mutations in genes involved in the rat sarcoma/mitogen‐activated protein kinases (RAS/MAPK) pathway. Historically, RASopathies have been described by clinical phenotypes, such as Noonan syndrome and Neurofibromatosis type I.
Anastasia‐Vasiliki Madenidou, Gillian I. Rice, James O'Sullivan, Ben Parker, Ian N. Bruce, Emma Burkitt‐Wright, Tracy A. Briggs   +6 more
wiley   +1 more source

Glucagon‐Like Peptide 1 Receptor Agonists, Sodium‐Glucose Cotransporter 2 Inhibitors, and Risk of Autoimmune Rheumatic Diseases

Arthritis &Rheumatology, EarlyView.
Objective Glucagon‐like peptide 1 receptor agonists (GLP‐1RAs) and sodium‐glucose cotransporter 2 inhibitors (SGLT2i) facilitate weight loss and exhibit immunomodulatory effects, but their impact on the risk of developing autoimmune rheumatic diseases (ARDs) is unclear.
Derin Karacabeyli, Diane Lacaille, Na Lu, Hui Xie, J. Antonio Aviña‐Zubieta   +4 more
wiley   +1 more source

2022 American College of Rheumatology/EULAR Classification Criteria for Takayasu Arteritis [PDF]

, 2022
Peter C. Grayson, Cristina Ponte, Ravi Suppiah, Joanna Robson, Katherine Gribbons, Andrew Judge, Anthea Craven, Sara Khalid, Andrew Hutchings, Debashish Danda, Raashid Luqmani, Richard A. Watts, Peter A. Merkel, for the DCVAS Study Group   +13 more
openalex   +3 more sources

Typhoid-associated acute kidney injury masquerading as a relapse of Takayasu arteritis

Saudi Journal of Kidney Diseases and Transplantation, 2017
Renal dysfunction is common in Takayasu arteritis. Uncommonly, renal failure in a case of Takayasu arteritis can be due to an unrelated disease, and if the disease is a rare complication, it is even more difficult to diagnose.
Revanasiddappa Manjunath, Anupama Kaul, Raj Kumar Sharma, Dharmendra Singh Bhadauria, Narayan Prasad, Amit Gupta   +5 more
doaj   +1 more source

Aortic valve replacement surgery for a case of infantile Takayasu arteritis [PDF]

Korean Journal of Pediatrics, 2012
Takayasu arteritis is a chronic inflammatory disease of unknown etiology primarily affecting the aorta and its major branches and usually occurring in the second or third decade of life.
Hye Won Kwon, Yoon Jung Suh, Ji Seok Bang, Bo Sang Kwon, Gi Beom Kim, Eun Jung Bae, Woong Han Kim, Chung Il Noh   +7 more
doaj   +1 more source

A multifaceted interplay between hemophagocytosis, IL‐18 and type I IFN distinguishes Still disease from other autoinflammatory diseases

Arthritis &Rheumatology, Accepted Article.
Objectives The unknown pathophysiology and the lack of specific features for systemic Juvenile Idiopathic arthritis and adult‐onset Still disease (collectively Still disease/SD) delays diagnosis and appropriate treatment. The goal of this study was to identify features and mechanisms that distinguish SD from other systemic autoinflammatory diseases ...
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, ImmunAID consortium, Vassili Soumelis, Bruno Fautrel, Cem Gabay, Peter D. Katsikis   +17 more
wiley   +1 more source

Bronchiectasis and hoarseness of voice in takayasu arteritis: a rare presentation

BMC Research Notes, 2012
Background Takayasu arteritis is a large vessel vasculitis occurring in young females. We report a rare presentation of Takayasu arteritis in a Sri Lankan woman.
ND Perera Gamage, C Jayasinghe Anusha, D Dias Lalindra, Kulatunga Aruna   +3 more
doaj   +1 more source