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Morquio Syndrome, sources - Coggle Diagram
Morquio Syndrome
Where was Morquio Syndrome discovered?
It was described by Luis Morquio a Uruguayan physician and a pediatrician in Montevideo, Uruguay.
Morquio Syndrome was first described independently in 1929.
He was born on September 24,1867 at Montevideo, Uruguay and died on June 19, 1935 at the age of 67.
What is Morquio Syndrome?
Morquio Syndrome is a rare genetic condition that affects a child’s bones, spine, and physical abilities.
These chains accumulate in cells, blood, tendons, and ligaments, causing damage over time.
Children with this condition are missing or don’t produce enough of the enzymes that break down sugar chains naturally produced in the body.
When does Morquio Syndrome start showing up in a persons body?
The symptoms usually begin between ages 1 and 3.
Morquio syndrome is a progressive disease, meaning symptoms get worse as a child grows.
The disease may not be visible at birth
How did Morquio syndrome get its name?
Why are people with Morquio Syndrome so short?
And also skeletal dysplasia, a condition that affects the .growth of cartilage and bone
They are so short because their bodies cannot properly break down certain sugar molecules
The frequency of Morquio syndrome is one in 200,000 births.
It was first described by Luis Morquio in 1919.
Who gets Morquio Syndrome?
Both parents must carry the gene and pass it to the child.
Morquio syndrome is a recessive genetic condition
https://www.childrenshospital.org/conditions/morquio-syndrome
https://www.chop.edu/conditions-diseases/morquio-syndrome
https://www.nemours.org/services/morquio-syndrome/about-morquio-syndrome.html#:~:text=Morquio%20syndrome%20is%20another%20name,by%20Luis%20Morquio%20in%201919.&text=The%20frequency%20of%20Morquio%20syndrome,Learn%20more%20about%20treatment%20options
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