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 Neuromuscular Disorders (e.g., ALS/Lou Gehrig's Disease)

Limb-girdle muscular dystrophies

Limb-girdle muscular dystrophies

Superficial anterior muscles
Superficial anterior muscles

Definition:

Limb-girdle muscular dystrophies include at least 10 different inherited disorders, which initially affect the muscles around the shoulder girdle and the hips. These diseases are progressive and may involve other muscles over a period of time.

Alternative Names:
Muscular dystrophy - limb-girdle type
Causes, incidence, and risk factors:

This is a large group of genetic diseases featuring muscle weakness and wasting (muscular dystrophy). Most are inherited in an autosomal recessive manner (both parents must pass on the defective gene for a child to have the disease), but some are autosomal dominant (only one parent needs to pass on the bad gene to affect the child). For some of these conditions, the defective gene has been discovered, but for others, the gene is not yet known.

Typically, the first sign is pelvic muscle weakness (difficulty standing from a sitting position without using arms, difficulty climbing stairs), which starts in childhood to young adulthood. Later there is the shoulder weakness. The disease will cause significant loss of mobility or wheelchair dependence over the next 20-30 years.

An important risk factor is having a family member with muscular dystrophy.

Symptoms:
  • Muscle weakness in pelvis, hips, upper legs, shoulders
  • Loss of muscle mass in the same areas, thinning of those body parts
  • Low back pain
  • Abnormal, sometimes waddling, gait while walking
  • Later in disease, there can be facial muscle weakness
  • Later in the disease, muscles of the lower legs, feet, lower arms, and hands can become weak
  • Late in the disease, there can be contractures of joints (they become fixed in a contracted position)
  • Palpitations or passing out spells can be caused by abnormal heart rhythms
  • Sometimes the calves will look large and muscular (pseudohypertrophy), but they are actually not strong
Signs and tests:
  • Normal muscle biopsy for dystrophin (the protein that is defective in the more common Duchenne muscular dystrophy)
  • Electromyogram (EMG) testing shows a pattern called myopathy, sick and dying muscle fibers
  • High blood creatine kinase levels
  • Muscle biopsy shows deteriorating muscle, with splitting of muscle fibers and the presence of cells of the immune system (phagocytes), which are not normally present
  • In some less common muscular dystrophies, the heart may show weakness (heart failure) on echocardiogram, or an abnormal rhythm on ECG

Review Date: 8/11/2006
Reviewed By: Brian Kirmse, MD, Mount Sinai School of Medicine, Department of Human Genetics, New York, NY. Review provided by VeriMed Healthcare Network.

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 Limb-girdle muscular dystrophies

   
   

 

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