Systemic manifestations and symptom burden of facioscapulohumeral muscular dystrophy in a referral cohort

Keyphrases

• Symptom Burden 100%
• Facioscapulohumeral muscular Dystrophy 100%
• Systemic Symptoms 100%
• Systemic Manifestations 100%
• Clinical Phenotype 25%
• Sensorineural Hearing Loss 25%
• Diagnostic Test 12%
• Patient Response 12%
• Age of Onset 12%
• Population-based Study 12%
• Genetic Disease 12%
• Neurologist 12%
• Ventricular Arrhythmia 12%
• Genetic Profile 12%
• Headache 12%
• Disease Duration 12%
• Echocardiogram 12%
• Cardiac Disease 12%
• Disease Manifestations 12%
• Dysphagia 12%
• Skeletal muscle Weakness 12%
• Large Series 12%
• Respiratory Insufficiency 12%
• Ocular Pathology 12%
• Ocular Abnormalities 12%
• Retrospective Chart Review 12%
• Cardiac Conduction 12%
• Forced Vital Capacity 12%
• Oropharyngeal Dysphagia 12%
• Conduction Defects 12%
• Difficulty Sleeping 12%
• Patient numbers 12%
• Disease Age 12%

Medicine and Dentistry

• Patient Referral 100%
• Facioscapulohumeral Muscular Dystrophy 100%
• Sensorineural Hearing Loss 25%
• Diseases 25%
• Onset Age 12%
• Respiratory Failure 12%
• Echocardiography 12%
• Eye Disease 12%
• Headache 12%
• Heart Disease 12%
• Muscle Weakness 12%
• Arrhythmia 12%
• Plummer-Vinson Syndrome 12%
• Disease Duration 12%
• Ocular Pathology 12%
• Forced Vital Capacity 12%
• Oropharyngeal Dysphagia 12%
• Heart Muscle Conduction Disturbance 12%
• Mood Change 12%
• Cardiac Conduction 12%
• Skeletal Muscle 12%
• Diagnostic Testing 12%
• Genetics 12%
• Alertness 12%