We report right here on a 61-year-old affected person with acute proper coronary heart failure of unclear etiology. Echocardiography revealed a myocardial mass infiltrating the
Year: 2021
Coexistence of disseminated tuberculosis and peripheral deep vein thrombosis in a child with newly diagnosed celiac disease: A rare entity
Some case experiences have been printed suggesting affiliation of celiac illness (CD) with tuberculosis (TB) and with deep vein thrombosis (DVT) however principally in grownup
Public and patient involvement in health data governance (DATAGov): protocol of a people-centred, mixed-methods study on data use and sharing for rare diseases care and research
Worldwide coverage imperatives for the general public and affected person involvement within the governance of well being knowledge coexist with conflicting cross-border insurance policies on
Challenges in Transition From Childhood to Adulthood Care in Rare Metabolic Diseases: Results From the First Multi-Center European Survey
Inherited Metabolic Illnesses (IMDs) are uncommon ailments attributable to genetic defects in biochemical pathways. Earlier prognosis and advances in therapy have improved the life expectancy
Effects of Teleassistance on the Quality of Life of People With Rare Neuromuscular Diseases According to Their Degree of Disability
Uncommon neuromuscular illnesses (RNMDs) are a gaggle of pathologies characterised by a progressive lack of muscular power, atrophy, fatigue, and different muscle-related signs, which have
The interoperability between the Spanish version of the International Classification of Diseases and ORPHAcodes: towards better identification of rare diseases
Uncommon ailments current a large spectrum of scientific manifestations and severity ranges and are sometimes poorly recognized and underrepresented, making them tough to categorise. Diagnoses