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Facioscapulohumeral muscular dystrophy - MedlinePlus Facioscapulohumeral muscular dystrophy is a disorder characterized by muscle weakness and wasting (atrophy) This condition gets its name from the muscles that are affected most often: those of the face (facio-), around the shoulder blades (scapulo-), and in the upper arms (humeral)
Facioscapulohumeral Muscular Dystrophy (FSH, FSHD) What is facioscapulohumeral muscular dystrophy? Facioscapulohumeral muscular dystrophy (FSHD) is a genetic muscle disorder in which the muscles of the face, shoulder blades, and upper arms are among the most affected
FSHD (Facioscapulohumeral Muscular Dystrophy): Symptoms Facioscapulohumeral muscular dystrophy (FSHD) is an inherited disease that often affects muscles in your face and upper body but can spread to any muscle in your body Symptoms typically develop between adolescence and age 20 to 30 There’s no cure for FSHD, but there are therapies to ease your symptoms and help you keep up your quality of life
Facioscapulohumeral Muscular Dystrophy - StatPearls - NCBI Bookshelf Facioscapulohumeral muscular dystrophy (FSHD) is a genetic illness inherited in an autosomal dominant fashion that affects skeletal muscle tissue in affected individuals Muscle groups involved include those of the face, shoulder girdle, and lower extremity affected asymmetrically
Facioscapulohumeral muscular dystrophy (FSHD) Facioscapulohumeral muscular dystrophy (FSHD) is a genetic condition that causes progressive muscle weakness that primarily affects the face, shoulders, and upper arms Learn about symptoms, diagnosis, and management
Facioscapulohumeral Muscular Dystrophy: Treatment and More What Is Facioscapulohumeral Muscular Dystrophy? Facioscapulohumeral muscular dystrophy (FSHD) is the third most common type of muscular dystrophy Although it also causes progressive muscle weakness, FSHD does not shorten your life expectancy as other forms of muscular dystrophy do
Facioscapulohumeral muscular dystrophy - Wikipedia Facioscapulohumeral muscular dystrophy (FSHD) is a type of muscular dystrophy, a group of heritable diseases that cause degeneration of muscle and progressive weakness
Facioscapulohumeral Muscular Dystrophy - PMC Facioscapulohumeral muscular dystrophy has a characteristic descending pattern of weakness, first affecting the face and shoulder followed by the distal lower extremity and the proximal hip girdle muscles, but many variations in presentation can occur
Facioscapulohumeral muscular dystrophy - UpToDate It is a complex genetic disorder characterized in most cases by slowly progressive muscle weakness involving the facial, scapular, upper arm, lower leg, and hip girdle muscles, usually with asymmetric involvement The clinical aspects of facioscapulohumeral muscular dystrophies are discussed here
Facioscapulohumeral muscular dystrophy | About the Disease | GARD Facioscapulohumeral muscular dystrophy is a disorder characterized by muscle weakness and wasting (atrophy) This condition gets its name from the areas of the body that are affected most often: muscles in the face (facio-), around the shoulder blades (scapulo-), and in the upper arms (humeral)