What is Pompe disease?

About Pompe disease

• It is a rare inherited disorder that affects one child per million.
• Causes
  • Mutations in the GAA gene cause Pompe disease.
  • The GAA gene provides instructions for producing an enzyme called acid alpha-glucosidase (also known as acid maltase).
  • This enzyme is active in lysosomes, which are structures that serve as recycling centers within cells.
  • The enzyme normally breaks down glycogen into a simpler sugar called glucose, which is the main energy source for most cells.
  • Mutations in the GAA gene prevent acid alpha-glucosidase from breaking down glycogen effectively, which allows this sugar to build up to toxic levels in lysosomes.
  • This buildup damages organs and tissues throughout the body, particularly the muscles, leading to the progressive signs and symptoms of Pompe disease.
• Some common side effects and symptoms include muscle weakness, respiratory issues, heart problems and difficulty swallowing.
• This disease can be:
  • Infantile-onset: symptoms begin in the first few months after birth.
  • Late-onset or delayed-onset: symptoms appear later in childhood or in adulthood.
• It affects males and females equally.
• Treatment: The treatment includes enzyme replacement therapy (ERT).

Q1) What is enzyme?

An enzyme is a biological catalyst and is almost always a protein. It speeds up the rate of a specific chemical reaction in the cell. The enzyme is not destroyed during the reaction and is used over and over.

Source: Being Nidhi’s parents: A 24-year journey of joy and struggles with India’s ‘first’ Pompe disease patient

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