📚 StudyHub

🔬 Biology  ·  Locomotion and Movement  ·  NEET

What is muscular dystrophy?

  • A A chronic, slowly progressive degenerative disease that mainly affects the synovial joints throughout the body during normal conditions as generally observed
  • B A group of genetic diseases causing progressive muscle weakness and degeneration; most common is Duchenne MD caused by dystrophin gene mutation on X chromosome
  • C A disease that is sometimes thought to be caused mainly by a long-term, chronic dietary deficiency of vitamin D in typical laboratory settings under usual circumstances
  • D An autoimmune disorder in which the body's own circulating antibodies are sometimes thought to attack healthy muscle fibres according to most researchers

Correct answer: B. A group of genetic diseases causing progressive muscle weakness and degeneration; most common is Duchenne MD caused by dystrophin gene mutation on X chromosome

Explanation: Muscular dystrophy: genetic diseases affecting muscle proteins. Duchenne MD: X-linked recessive, mutation in DMD gene (largest human gene), lacks dystrophin (connects cytoskeleton to ECM), affects boys, progressive weakness from early childhood, loss of ambulation by teens. Becker MD: milder form with partial dystrophin function.

Concept context

Types of movement, muscle contraction, skeletal system, joints, and disorders. Important for Class 11 and NEET.

Read the full Locomotion and Movement notes →