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[COVID-19 vaccines efficacy and infection features in patients with systemic sclerosis: A single-center cohort study].
Beijing Da Xue Xue Bao Yi Xue Ban
December 2024
Department of Rheumatology and Immunology, Peking University People' s Hospital, Beijing 100044, China.
Objective: To comprehensively understand the COVID-19 vaccination and infection status among patients with systemic sclerosis (SSc).
Methods: We conducted a retrospective analysis of patients diagnosed with SSc who were hospitalized in the Rheumatology and Immunology Department of Peking University People' s Hospital from January 2016 to March 2023. We collected detailed clinical cha-racteristics, vaccination status, and infection details through a systematic review of medical records and telephone follow-ups with the SSc patients.
Age-Related Differences Between Juvenile and Adult Autoimmune Inflammatory Myopathies.
J Clin Rheumatol
December 2024
From the Division of Pediatric Rheumatology, Department of Pediatrics, University of Health Sciences, Ankara Bilkent City Hospital, Bilkent, Ankara, Turkey.
Background: Clinical features and prognosis of autoimmune inflammatory myopathies (AIMs) can vary depending on the age of disease onset. The aim of this study was to compare the demographic characteristics, clinical features, laboratory findings, and long-term prognosis of juvenile and adult AIMs.
Methods: Patients diagnosed with AIM between 2009 and 2023 in the pediatric rheumatology and rheumatology departments of our hospital were included in this medical records review study.
Type 1 Hyperphosphatemic Familial Tumoral Calcinosis Associated With a Homozygous Variant Mutation in the GALNT3 Gene.
Cureus
October 2024
Pediatrics, Armed Forces Hospital Southern Region, Khamis Mushait, SAU.
Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare genetic disorder characterized by abnormal phosphate metabolism leading to hyperphosphatemia and calcific deposits in soft tissues. Chronic recurrent multifocal osteomyelitis (CRMO) can be challenging to diagnose and manage, especially in the context of underlying genetic conditions. This case report presents a case of a 12-year-old girl with a complex presentation involving osteomyelitis and a rare genetic disorder.
View Article and Find Full Text PDFDacryoadenitis as a Rare Initial Presentation in a Patient with Suspected Crest Syndrome.
Eur J Case Rep Intern Med
September 2024
Department of Ophthalmology, Sawai Man Singh Medical College, Jaipur, India.
Article Synopsis
- Systemic sclerosis (SSc) is a rare disease that can affect different parts of the body, and this case is about a 51-year-old woman who had swelling in her eyelid.
- Doctors found she had an enlarged lacrimal gland and inflammatory symptoms that didn’t get better with regular treatments, which led them to explore further possible conditions.
- This case is important because it shows that SSc, specifically CREST syndrome, can have unusual symptoms like swelling in the eyes, and doctors need to think about different diagnoses when they see such signs.
Misdiagnosed Isolated Ruptured Mycotic Mitral Valve Aneurysm as Mitral Annulus Calcification.
Cardiovasc Hematol Disord Drug Targets
November 2024
Department of Cardiovascular Diseases, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Introduction: Subacute Bacterial Endocarditis (SBE) is a slowly developing type of infective endocarditis. Aneurysm is more common in this type of endocarditis. Currently, SBE is an uncommon cause of unexplained fever (FUO) because rapid diagnostic capabilities, such as echocardiography, have improved.
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