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.

Jun 26, 2023 · 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 …

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.

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 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).

Understanding FSHD. Facioscapulohumeral muscular dystrophy, or FSHD, is a genetic disorder that leads to the weakening of skeletal muscles. Typically beginning in early teenage years with the loss of muscles in the face (facio), shoulders (scapula), upper arms (humerus), legs or core, FSHD can spread to any muscle.

Jun 10, 2024 · Facioscapulohumeral muscular dystrophy (FSHD) is a chronic and progressive disease. It does not typically cause the severe disability and shortened lifespan seen with other dystrophies. However, people with more severe forms of the disease may still need to use a wheelchair or other aids eventually.

Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disease of the muscles. It causes your muscles to break down and weaken over time. It can develop quickly or slowly.

Facioscapulohumeral muscular dystrophy mainly affects the face, shoulder, and upper arm muscles. However, it can also affect muscles around the pelvis, hips, and lower leg. Symptoms can appear soon after birth (infantile form), but often they do not appear until age 10 to 26 years.

Usually, symptoms develop during the teen years, with most people noticing some problems by age 20, although weakness in some muscles can begin as early as infancy and as late as the 50s. In some people, the disease can be so mild that no symptoms are noticed.