Morquio syndrome is a rare genetic condition that affects a child’s bones and spine, organs, and physical abilities. Children with this condition are missing or don’t produce enough of the enzymes that break down sugar chains naturally produced in the body. These chains accumulate in cells, blood, tendons, and ligaments, causing damage over time.
Symptoms & Causes
What are the symptoms of Morquio syndrome?
Signs and symptoms of Morquio syndrome typically appear between ages 1 and 3. Children with Morquio syndrome may develop:
Boston Children’s treats every child diagnosed with Morquio syndrome based on the symptoms. All children need monitoring. Orthopedic conditions like scoliosis, kyphosis, and leg deformities affect many children with Morquio syndrome and may require surgical intervention. A medication has been developed to help in the treatment of Morquio, but currently there is no cure. Based on your child’s symptoms, the care team may recommend careful monitoring or non-surgical treatment.
How we care for Morquio syndrome
Children with Morquio syndrome receive care from various specialists at Boston Children’s. Your child’s care team may include specialists from clinical genetics, orthopedics, pulmonology, and cardiology. Morquio syndrome is a progressive condition; your child’s medical needs may change over time. Her specialists at Boston Children’s work closely and carefully with each other and your family to ensure she receives the best care.
The Hematopoietic (Stem) Cell Transplant Program at Dana-Farber/Boston Children's Cancer and Blood Disorders Center is one of the largest and most experienced pediatric stem cell transplant programs in the world.