The Mystery Headache- Migraine, Positional Headache, Spinal Fluid Leak
Explore intracranial hypotension as a potential cause for chronic migraine-like symptoms that worsen when upright and improve when lying down, with insights on diagnosis and treatment options.
Diagnosis and Classification of Systemic Sclerosis (SSc) - Present and Future Challenges
Explore early diagnosis and classification of systemic sclerosis through expert insights, patient perspectives, and hospital pathways. Gain understanding of criteria, challenges, and future directions in SSc management.
Explaining Systemic Sclerosis (SSc) to Family and Friends
Gain insights on explaining systemic sclerosis to loved ones from patient representatives and experts. Learn to communicate effectively about this rare autoimmune disease and its impact.
Joint Hypermobility in Children: Approach and Diagnosis
Explore joint hypermobility in children, covering concepts, classification, diagnosis, and management. Learn to identify and investigate relevant cases effectively.
ERN ReCONNET Good Practice Sharing Initiative 2023 - First Edition
Explore innovative approaches in rare connective tissue disease care, including patient education, transition protocols, and specialized programs for conditions like Ehlers-Danlos syndrome and myositis.
Update on Hypermobile Type of Ehlers-Danlos Syndromes (EDS)
Explore hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders, including clinical boundaries, genetic diagnostics, and new findings on peripheral microcirculation and skin layers.
Marfan Syndrome vs. Ehlers-Danlos Syndrome - Biochemistry and Genetics
Explore the genetic and biochemical differences between Marfan Syndrome and Ehlers-Danlos Syndrome, focusing on connective tissue defects, symptoms, and clinical manifestations.
Scleroderma - CRASH! Medical Review Series
Explore the latest updates on scleroderma in this concise medical review, covering key aspects for physician licensing exam preparation and clinical understanding.
Marfan Syndrome - Causes, Symptoms, Diagnosis, and Treatment
Explore Marfan syndrome's genetic basis, symptoms, and treatment. Learn about its autosomal dominant inheritance, fibrillin-1 defects, and diverse clinical manifestations affecting connective tissues and organs.
Meet a Scleroderma Investigator - Natalie Saini's Research on Scleroderma Treatments
Explore groundbreaking scleroderma research with Dr. Natalie Saini, uncovering innovative approaches and potential breakthroughs in treatment and care for those affected by the disease.
Calcinosis in Scleroderma: Causes, Symptoms, and Treatment Options
Explore causes, symptoms, and treatments for calcinosis in scleroderma, including medications, lifestyle changes, and surgical interventions.
Musculoskeletal Manifestations in Systemic Sclerosis
Explore scleroderma's impact on the musculoskeletal system and learn strategies to manage joint pain and improve function with expert insights.
Skin Manifestations and Skin Care in Scleroderma
Explore skin manifestations and care strategies for scleroderma with expert insights from dermatologists Dr. Lam and Dr. Gonzalez.
Ehlers-Danlos Syndromes and Hypermobile Spectrum Disorders
Gain insights into Ehlers-Danlos Syndromes and hypermobile spectrum disorders through an expert medical presentation from Johns Hopkins, covering diagnostic criteria and clinical implications.