Muscle Dystrophy Overview and Symptoms
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Questions and Answers

What is the main sign of muscular dystrophy?

  • Delayed growth
  • Development of scoliosis
  • Progressive muscle weakness (correct)
  • Facial paresis

What is a common treatment option for muscular dystrophy?

  • Acupuncture
  • Radiation therapy
  • Chemotherapy
  • Medications (correct)

Which of the following might indicate advanced muscular dystrophy?

  • Frequent falls (correct)
  • Strong muscle tone
  • Heightened reflexes
  • Ability to run long distances

Which genetic pattern is described when a mutation is inherited from one parent?

<p>Autosomal Dominant (A)</p> Signup and view all the answers

What can be a potential complication associated with muscular dystrophy?

<p>Cognitive impairment (B)</p> Signup and view all the answers

What is the frequency at which all types of muscular dystrophy combined affect individuals?

<p>16 to 25 per 100,000 (D)</p> Signup and view all the answers

What age do many patients with muscular dystrophy become wheelchair dependent?

<p>By age 12 (A)</p> Signup and view all the answers

Which symptom is least likely associated with muscular dystrophy?

<p>Enhanced cognitive function (A)</p> Signup and view all the answers

Which method is commonly used to test for muscular dystrophy?

<p>Blood test and muscle biopsy (B)</p> Signup and view all the answers

What is a typical prognosis for patients with muscular dystrophy?

<p>Poor, with many dependent on wheelchairs by age 12 (B)</p> Signup and view all the answers

Muscular dystrophies cause progressive weakness and breakdown of skeletal muscles over time.

<p>True (A)</p> Signup and view all the answers

The main sign of muscular dystrophy is sudden muscle strength improvement.

<p>False (B)</p> Signup and view all the answers

Patients with muscular dystrophy are often wheelchair dependent by the age of 12.

<p>True (A)</p> Signup and view all the answers

Learning disabilities are not associated with muscular dystrophy.

<p>False (B)</p> Signup and view all the answers

Scoliosis can be a possible disability resulting from muscular dystrophy.

<p>True (A)</p> Signup and view all the answers

Both parents having the mutation guarantees that their child will have muscular dystrophy.

<p>False (B)</p> Signup and view all the answers

Facial paresis can be a symptom of muscular dystrophy.

<p>True (A)</p> Signup and view all the answers

Bradley Walker and Steve Tillian are notable figures with muscular dystrophy.

<p>True (A)</p> Signup and view all the answers

Treatment options for muscular dystrophy do not include physical therapy.

<p>False (B)</p> Signup and view all the answers

The prognosis for patients with muscular dystrophy is typically poor.

<p>True (A)</p> Signup and view all the answers

Flashcards

What is Muscular Dystrophy?

Muscular dystrophies are a group of rare genetic diseases that cause progressive muscle weakness and breakdown over time.

Types of Gene Mutations

Muscular Dystrophy can be caused by different types of gene mutations. Autosomal dominant mutations are inherited from one parent, while X-linked mutations are passed from a mother to her son.

Main Symptoms

The main symptom of Muscular Dystrophy is progressive muscle weakness, leading to difficulty with activities like running, jumping, and rising from a sitting or lying position.

Prognosis

The prognosis of Muscular Dystrophy is typically poor, with most patients becoming wheelchair-dependent by the age of 12, and death often occurring due to respiratory or cardiac complications.

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Treatment Options

Treatment for Muscular Dystrophy includes medications, physical therapy, occupational therapy, and surgical procedures, with the goal of slowing the progression of the condition.

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What is a Muscle Biopsy?

A muscle biopsy is a procedure where a small sample of muscle tissue is taken to be examined under a microscope, helping doctors diagnose Muscular Dystrophy.

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What is Scoliosis?

Scoliosis is a condition where the spine curves abnormally, which can occur in some cases of Muscular Dystrophy.

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What are Learning Disabilities?

Learning disabilities can occur in some individuals with Muscular Dystrophy, impacting cognitive function.

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How common is Muscular Dystrophy?

The combined prevalence of all types of Muscular Dystrophy is estimated to be approximately 16 to 25 per 100,000 people.

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What are Muscular Dystrophies?

Muscular dystrophies are a group of rare genetic diseases that cause progressive muscle weakness and breakdown over time. They are caused by gene mutations affecting muscle proteins.

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Causes of Muscular Dystrophy

Muscular dystrophy can be caused by different types of gene mutations. Autosomal dominant: inherited from one parent. X-linked: passed from a mother to her son.

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Main Symptom of MD

The main symptom of Muscular Dystrophy is progressive muscle weakness, leading to difficulty with activities like running, jumping, and rising from a sitting or lying position.

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Other Signs of Muscular Dystrophy

Apart from weakness, MD can cause frequent falls, muscle pain, delayed growth, learning disabilities, and walking on toes.

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Prognosis of Muscular Dystrophy

The prognosis of Muscular Dystrophy is typically poor, with most patients becoming wheelchair-dependent by the age of 12, and death often occurring due to respiratory or cardiac complications.

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How is Muscular Dystrophy Diagnosed?

Doctors diagnose Muscular Dystrophy through blood tests and muscle biopsies. These tests help identify gene mutations and muscle abnormalities.

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Treatment for Muscular Dystrophy

Treatment for Muscular Dystrophy includes medications, physical therapy, occupational therapy, and surgical procedures, with the goal of slowing the progression of the condition.

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Learning Disabilities and Muscular Dystrophy

Learning disabilities can occur in some individuals with Muscular Dystrophy, impacting cognitive function and learning abilities.

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Prevalence of Muscular Dystrophy

The combined prevalence of all types of Muscular Dystrophy is estimated to be approximately 16 to 25 per 100,000 people.

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Study Notes

Muscle Dystrophy Overview

  • Muscle dystrophies are genetically diverse and rare neuromuscular disorders
  • Characterized by progressive weakness and muscle breakdown
  • Symptoms vary, but typically affect skeletal muscles over time

Causes of Muscle Dystrophy

  • Primarily caused by gene mutations affecting muscle proteins
  • Genetic inheritance:
    • Autosomal dominant: When a mutation is inherited from a parent
    • X-linked: When the genetic change is passed down through X chromosomes

Symptoms of Muscle Dystrophy

  • Specific symptoms appear at different ages and affect different muscle groups
  • Common symptoms include:
    • Frequent falls
    • Difficulty rising from a lying position
    • Trouble running and jumping
    • Muscle pain
    • Delayed growth
    • Learning disabilities
    • Walking on toes
    • Scoliosis
    • Enlarged calves
    • Facial paresis

Prognosis of Muscle Dystrophy

  • Typically, the prognosis is poor.
  • Patients often rely on wheelchairs by age 12
  • Death commonly results from respiratory or cardiac complications

Treatment of Muscle Dystrophy

  • Treatment options include:
    • Medications
    • Physical therapy
    • Occupational therapy
    • Surgical procedures

Possible Disabilities

  • Potential disabilities include:
    • Scoliosis
    • Learning disabilities
    • Enlarged calves
    • Difficulty rising from the floor
    • Facial paresis
    • Frequent falls
    • Cognitive impairment
    • Problems with swallowing

Facts about Muscle Dystrophy

  • Diagnostic tools: Blood tests and muscle biopsies are used
  • Doctors identify different types of Muscular Dystrophy
  • The combined effect of all types is about 16 to 25 cases per 100,000 individuals
  • Heart failure from the total reported cases contributes 20%
  • Respiratory failure contributes 31 % of reported deaths
  • One baby is born with MD out of 20,000 births
  • Recommended diet: High protein, low fat, and low carbohydrates.
  • Different muscle types are affected by various muscular dystrophy types
  • Some muscle groups such as in the heart and controlling breathing may be weak
  • No cure; physical therapy may help manage symptoms

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Description

This quiz covers the essential aspects of muscle dystrophies, including their genetic causes, symptoms, and prognosis. Learn about the different types of muscle dystrophies and how they affect muscle function over time. Test your knowledge on this rare neuromuscular disorder.

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