Also known as: MPS IV.
What is Morquio syndrome?
Morquio syndrome is a genetic disorder where a baby has trouble breaking down sugar chains in the body. This prevents the body from getting the required nutrients for the development of things like skin, tendons, ligaments, bone, cartilage and other tissues. It can lead to a number of potential complications.
What causes Morquio syndrome?
Morquio syndrome is a hereditary condition that is passed down from parents to children.
What are the symptoms of Morquio syndrome?
The problems tied to Morquio syndrome lead to symptoms such as curved spine (scoliosis), joints that move more than they should (hypermobility), neck that moves more than it should (instability), a large head, short stature, wide teeth, heart and vision problems and a number of other complications.
What are Morquio syndrome care options?
Morquio syndrome cannot be cured. The treatments can vary widely depending on what parts of the body are affected. Treatment may include physical therapy, occupational therapy, counseling, surgery and other treatments.
Reviewed by: Stephen Graham George Jr., MD
This page was last updated on: 8/13/2018 10:41:47 AM
From the Newsdesk
Nicklaus Children's Hospital will be one of a handful in the country to offer a fast turn-around on genome sequencing that can be a key to saving infants with rare and hard-to-diagnose genetic disorders. As seen on The Miami Herald.
Enzymes are particularly important in the processing of medicines and drugs. They determine how our bodies are going to handle the medicines we take, and if those medicines are going to help us feel better or not. This research study includes testing the status of the CYP2D6 gene in children.