Isabel has mucopolysaccharidosis type VI, also known as Maroteaux-Lamy syndrome or MPS-6, and she was part of a medical trial that saved her life years ago ...

Severe Maroteaux–Lamy syndrome (mucopoly- saccharidosis type VI) is usually fatal by early adulthood. Bone marrow transplantation is the only form of definitive enzyme replacement therapy available.

Her deteriorating health baffled her doctors in Guatemala, who sent her to the United States, where she received a terrifying diagnosis: the exceedingly rare Maroteaux-Lamy syndrome. “My life ...

In 1997 the team developed the only treatment for Maroteaux-Lamy Syndrome. But tens of millions of dollars were required to take it to the next stage - clinical trials, and an American drug ...

Isabel Bueso, 24, is battling a genetic disorder known as Maroteaux-Lamy Syndrome or Mucopolysaccharidosis Type VI. In 2003, she and her family left Guatemala and came to the U.S. legally, so she ...

The Chicago native had Maroteaux-Lamy syndrome and was scheduled to undergo heart surgery earlier this month. By Scottie Andrew, CNN, CNNWire. Saturday, December 31, 2022.

Maroteaux Lamy Syndrome News and Research RSS. Genetic Disorder Tracker introduced by Guidepoint Global. Guidepoint Global, LLC, a leading primary research firm, ...

Maria Isabel Bueso, who goes by Isabel, has an extremely rare condition known as Maroteaux-Lamy Syndrome that confines her to a wheelchair and requires that she use a medical device to breathe. She ...

When Kendra Gottsleben was growing up, she wore dresses made by her grandmother. Many grandmothers care for their grandchildren this way, but Gottsleben was born with Maroteaux-Lamy syndrome, a ...