Becker Muscular Dystrophy

Reports from the MHC data base

Report from the Observation Chart (PDF)

Codes

ICD-10: G71.0B
ORPHA: 98895

Estimated occurrence

4:100 000 male inhabitants

Etiology

The disease is caused by a mutation in the dystrophin gene. The type of mutations occur ring in Becker muscular dystrophy results in severe deficiencies of the protein dystrophin in the muscle fibers. Dystrophin is important for muscle fiber cohesion. The absence of dystrophin renders the muscle fibers more susceptible to degeneratation. The dystrophy gene is located on the X chromosome. In about a third of the cases, the disease is caused by a new mutation.

General symptoms

The symptoms associated with Becker muscular dystrophy closely resemble those of Duchenne muscular dystrophy but are milder. Pronounced symptoms may however sometimes occur. Although muscle weakness is observed in a few cases during infancy, symptoms appear much later in many. Muscle weakness nearly always begins in the legs. About 20% of the cases will require some aid of a wheelchair; the age at which this occurs greatly varies. Muscle weakness also often progresses with age to the upper body and arms. As dystrophin is normally found in the skeletal musculature and heart muscle, as well as to a lesser degree in the central nervous system, symptoms from the heart and central nervous system may occur. Most have no symptoms from the respiratory tract.

Orofacial/odontological symptoms

Muscle weakness in the masticatory and facial muscles, especially if occurring at an early age, may lead to malocclusions. Muscle strength and endurance in the masticatory musculature may gradually decrease. It then becomes more difficult to masticate food, which in turn may eventually lead to altered dietary habits. In cases of reduced muscle strength in the arms and hands, toothbrushing may be difficult.

Orofacial/odontological treatment

  • Problems in managing toothbrushing and dental care due to tired and weak arm and jaw muscles justify extra prophylactic dental care.
  • An or thodontist should be consulted between the ages of 7 and 9 in order to identify dental aberrations or malocclusions and to plan any necessary orthodontic treatment.
  • Orofacial assistive devices should be tried when needed; among these, an electric toothbrush may be of great help.
  • Eating difficulties should be investigated and treated by a specialist team.

Sources

  • The rare disease database of the Swedish National Board of Health and Welfare.
  • The MHC database - The Mun-H-Center database on oral health and orofacial function in rare diseases.
Updated: 2017-09-12 13:39