We are independent & ad-supported. We may earn a commission for purchases made through our links.
Advertiser Disclosure
Our website is an independent, advertising-supported platform. We provide our content free of charge to our readers, and to keep it that way, we rely on revenue generated through advertisements and affiliate partnerships. This means that when you click on certain links on our site and make a purchase, we may earn a commission. Learn more.
How We Make Money
We sustain our operations through affiliate commissions and advertising. If you click on an affiliate link and make a purchase, we may receive a commission from the merchant at no additional cost to you. We also display advertisements on our website, which help generate revenue to support our work and keep our content free for readers. Our editorial team operates independently of our advertising and affiliate partnerships to ensure that our content remains unbiased and focused on providing you with the best information and recommendations based on thorough research and honest evaluations. To remain transparent, we’ve provided a list of our current affiliate partners here.
Health

Our Promise to you

Founded in 2002, our company has been a trusted resource for readers seeking informative and engaging content. Our dedication to quality remains unwavering—and will never change. We follow a strict editorial policy, ensuring that our content is authored by highly qualified professionals and edited by subject matter experts. This guarantees that everything we publish is objective, accurate, and trustworthy.

Over the years, we've refined our approach to cover a wide range of topics, providing readers with reliable and practical advice to enhance their knowledge and skills. That's why millions of readers turn to us each year. Join us in celebrating the joy of learning, guided by standards you can trust.

What Is Maroteaux Lamy Syndrome?

By Meshell Powell
Updated: May 17, 2024
Views: 4,582
Share

Maroteaux Lamy syndrome is a rare genetic metabolic disorder that is named after the French doctors who first described the condition. Some of the most common symptoms associated with Maroteaux Lamy syndrome include delayed growth, joint stiffness, and bone abnormalities. Heart disease and the presence of hernias are also common among those with this disorder. Although there is no cure for this medical condition, enzyme replacement therapy can be useful in helping to manage the illness. Any individualized questions or concerns about Maroteaux Lamy syndrome should be discussed with a doctor or other medical professional.

This condition is caused by a recessive gene, meaning that both parents must be a carrier for the gene that is responsible for Maroteaux Lamy syndrome. It is possible to be a carrier for the defective gene without actually having the condition itself. A child born to parents who both carry this defective gene has a one in four chance of developing the condition.

The symptoms of Maroteaux Lamy syndrome are all physical in nature, as intellect is not typically affected. One of the first signs that something is not quite normal is a delayed ability learning to walk. Additional tests may reveal restricted joint movement and abnormalities involving the shape of some bones, particularly those of the spine. In the more severe cases, the abdomen may protrude significantly.

Many people with Maroteaux Lamy syndrome are diagnosed at some point with a hernia, or a protrusion of part of the intestine through the abdominal wall. Surgery is typically needed to repair the hernia in order to prevent potentially life-threatening complications. Heart disease or other cardiac issues are extremely common, as the majority of those who are diagnosed with this condition will develop some form of heart malfunction, usually involving at least one defective heart valve. Surgical intervention may be needed in order to repair damage to the heart, although this method of treatment is usually delayed as much as possible due to the risks associated with heart surgery,

There is no cure for Maroteaux Lamy syndrome, and treatment is aimed at easing specific symptoms. Potentially serious problems such as heart issues or the development of hernias usually requires surgical intervention. Supportive devices such as braces, crutches, or wheelchairs may be used in an effort to increase mobility and independence. Other symptoms are treated on an as-needed basis, making clear and frequent communication with the supervising physician very important.

Share
WiseGeek is dedicated to providing accurate and trustworthy information. We carefully select reputable sources and employ a rigorous fact-checking process to maintain the highest standards. To learn more about our commitment to accuracy, read our editorial process.

Editors' Picks

Discussion Comments
Share
https://www.wisegeek.net/what-is-maroteaux-lamy-syndrome.htm
Copy this link
WiseGeek, in your inbox

Our latest articles, guides, and more, delivered daily.

WiseGeek, in your inbox

Our latest articles, guides, and more, delivered daily.