1. Abstract Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome is an uncommon but potentially life-threatening form of adverse drug reaction (ADR), most frequently reported with antiepileptics and antibiotics.
1. Abstract Gadolinium-ethoxybenzyl-diethylene-triamine-pentaacetic acid (Gd EOB-DTPA) MRI has the advantage of simultaneously screening for hepatocellular carcinoma (HCC) and evaluating liver damage due to Fontan associated liver disease (FALD), and is suitable.
1. Abstract A 35-year-old woman was treated for complete dysphagia resulting from a chemical burn of the esophagus. Between 2012 and 2019, numerous interventional gastroscopies (4–16 per year) were performed to alleviate her sympoms.
1. Abstract 1.1. Background Although long-term antiviral therapy for chronic hepatitis B virus (HBV) can reverse fibrosis even in patients with liver cirrhosis, fibro sis progression can still occur despite viral suppression.
1. Abstract Purple Urine Bag Syndrome (PUBS) is a rare condition observed in patients with long-term catheterization, often manifesting as a purple discoloration of urine within the catheter bag.
1. Abstract 1.1. Aim This study aimed to develop a predictive signature based on mitophagy-related lncRNAs to assess their prognostic and immunological significance in STAD patients.
1. Abstract Obesity is a disease that affects a large part of the world’s population. With associated comorbidities, such as cardiorespiratory diseases, diabetes and mobility difficulties, interventions, among which robotic bariatric surgery emerges as promising.
1. Abstract 1.1. Objective This study aimed to use a randomised controlled trial to evaluate and compare the endoscopic morphological characteristics and patholog ic types of colorectal polyps between water-immersion and air-insufflation colonoscopy.
1. Introduction Cornelia de Lange Syndrome (CdLS) is a rare genetic disease (OMIM#122470, #300590, #300882, #614701, #610759), with a broad phenotypic spectrum, including congenital malformations, neurodevelopmental delay, intellectual disability, and behavioral disorders [1,2].
1. Short Communication Acrocallosal Syndrome (ACS) is a monogenic, autosomal recessive condition, with intellectual disability, dysmorphic facial features, cen-tral nervous system abnormalities and distal limb malformations.
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