mucopolysaccharidosis
/ˌmjuːkoʊˌpɒliˌsækəraɪˈdoʊsɪs/
noun
- A group of rare genetic disorders in which the body cannot break down certain sugar molecules, leading to buildup in cells and tissues and causing various health problems.
- Treatment for mucopolysaccharidosis often includes enzyme replacement therapy to help break down the accumulated sugars.
- Mucopolysaccharidosis type I, also known as Hurler syndrome, can affect the heart, bones, and brain.
- Doctors diagnosed the child with mucopolysaccharidosis after noticing delayed growth and stiff joints.