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Information About Muscular Dystrophy

We Have to Know about the Muscular Dystrophy

  • Muscular dystrophy (MD) is a group of inherited muscle diseases in which muscle fibers are unusually at risk of damage.
  • Muscles, mainly voluntary muscles, become progressively weaker.
  • Some forms of the genetic disorder have an effect on heart muscles, other involuntary muscles, and other organs.
  • There’s no cure for muscular dystrophy, but medications and therapy can slow the course of the disease.

Causes of Muscular Dystrophy

  • The most common types of muscular dystrophy appear to be due to a genetic deficiency of the muscle protein dystrophy.

Signs & Symptoms of Muscular Dystrophy

Signs and symptoms generally seem in time of life and will include:

  • Frequent falls
  • The difficulty arising from a lying / sitting up position
  • Trouble running and jumping
  • Waddling gait
  • Walking on the toes
  • Large calf muscles
  • Muscle pain and stiffness
  • Learning disabilities

Doof Muscular Dystrophy

  • consult the doctor

Medical advice for Muscular Dystrophy

  • Duchenne’s genetic disorder happens virtually completely in boys, although it can occur in girls. Your young child may have difficulty walking, running, rising from the floor or climbing the stairs, or may appear clumsy and fall often. These may be early indications of muscular dystrophy (MD). A child with MD might learn to run later than alternative youngsters do and will exhibit signs of muscle weakness between the ages of two and half-dozen. By faculty age, a child with MD may walk unsteadily and on the toes or balls of the feet. Duchenne’s MD typically leads to youngsters losing the flexibility to run by age twelve.

See your doctor if you’re concerned about your child’s:

  • Motor abilities
  • Clumsiness
  • Muscle strength
  • Muscle development

Risk factors of Muscular dystrophy

  • Muscular dystrophy happens in each sex and altogether ages and races. However, the most common variety, Duchenne, usually occurs in young boys. People with a case history of sickness|genetic disorder|genetic abnormality|genetic defect|congenital disease|inherited disease|inherited disorder|hereditary disease|hereditary condition} square measure at higher risk of developing the disease or passing it on to their youngsters.

Treatment for Muscular Dystrophy

Currently, there is no cure for muscular dystrophy. Medications and numerous therapies facilitate slow the progression of the sickness and keep the patient mobile for the longest doable time.

Drugs

The two  most ordinarily prescription drugs for genetic disorder are:

  • Corticosteroids: This type of medication can help increase muscle strength and slow progression, but long-term use can weaken bones and increase weight gain.
  • Heart medications: If the condition impacts the heart, beta blockers and angiotensin-converting enzyme (ACE) inhibitors may help.

Physical therapy

  • General exercises: a spread of motion and stretching exercises will facilitate combat the inevitable inward movement of the limbs as muscles and tendons shorten. Limbs tend to become fixed in position, and these types of activities can help keep them mobile for longer. Standard low-impact aerobic exercises like walking and swimming may facilitate slow the disease’s progression.
  • Breathing assistance: because the muscles used for respiration become weaker, it may be necessary to use devices to help improve oxygen delivery through the night. In the most severe cases, a patient may need to use a ventilator to breathe on their behalf.
  • Mobility aids: Canes, wheelchairs, and walkers will facilitate the person to keep mobile.
  • Braces: These keep muscles and tendons stretched and facilitate slow their shortening. They conjointly offer supplementary support to the user once moving.

Self-care for Muscular Dystrophy

  • Exercise

Investigations for Muscular Dystrophy

  • Blood tests
  • Electromyography
  • Ultrasonography
  • Muscle biopsy
  • Genetic testing
Treatment for Muscular dystrophy
 Symptoms of Muscular dystrophy