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Alternative Names

GSD II; Glycogen Storage Disease Type II; Cardiomegalia Glycogenica Diffusa; Generalized Glycogenosis, Cardiac Form; Acid Maltase Deficiency; Acid Alpha-Glucosidase Deficiency; GAA Deficiency; Pompe Disease; Glycogenosis Type II; Alpha-1,4-Glucosidase Deficiency; Pompe's Disease; Pompes Disease

What is Pompe Disease?

Pompe disease, also known as glycogen storage disease type II, is an inherited disorder whose primary symptom is progressive weakness in the muscles used for mobility and breathing. In infants with Pompe disease, the heart muscles are often severely affected as well. These symptoms are caused by a mutation in an enzyme called alpha-glucosidase (also called maltase) that breaks down glycogen, a stored form of sugar used for energy. As a result, glycogen builds up in the body, notably in the muscles, and damages individual cells.

There are two main types of Pompe disease: infantile-onset and late-onset forms. The severity of symptoms, age at which symptoms begin, and rates of disease progression are related to the degree of alpha-glucosidase deficiency.

Infantile-onset Form

The infantile form is the most common and most severe type of Pompe disease. Babies with the disease may appear normal at birth, but begin to show symptoms in the first few months of life. They develop general muscle weakness and poor muscle tone, which causes their bodies to seem limp as they are unable to move, hold up their heads, or feed. They fail to gain weight and grow at the expected rate. Breathing problems can be compounded by lung infections. These infants have enlarged hearts and livers, and many also have enlarged tongues. The disease progresses rapidly and most infants with Pompe disease will die within the first year of life, often from heart or lung failure. In people with the infantile form of the disease, alpha-glucosidase is either entirely missing or inactive.

Late-onset Form

The late onset form of Pompe disease is due to a partial deficiency in alpha-glucosidase. Symptoms can begin at any time, from childhood to adulthood. In this form of the disease, muscle weakness eventually leads to breathing problems and death from lung failure. The heart may be involved, but it will not be enlarged. These people will lose mobility and eventually require a wheelchair or become bedridden. Machines may become necessary in order to breathe.

This form of the disease progresses more slowly, and life expectancy is better than in the infantile-onset form. People who develop symptoms of Pompe disease in late childhood often die in their 20s and 30s. Those who develop symptoms later may experience a slower progression, but unfortunately their lifespan will also be curtailed.

How Common is Pompe Disease?

Pompe disease affects roughly 1 in 100,000 people. The infantile-onset form is the most common type of Pompe disease.

How is Pompe Disease Treated?

In 2006, the FDA approved an enzyme replacement therapy to treat Pompe disease. Enzyme replacement therapy has been shown to decrease heart size, maintain normal heart function, and improve muscle tone and strength in people with the infantile-onset form of the disease. It is too soon to gauge how it will affect people with the disease long-term.

Clinical trials are being performed to study the effects of gene therapy in children with Pompe.

Adults and children with Pompe disease are often prescribed a protein-rich diet and a daily exercise regimen to help muscle tone and strength. They must also carefully monitor and treat lung infections.


Acid Maltase Deficiency Association

A non-profit aimed at funding research and promoting awareness of Pompe disease. The organization has numerous links on its website to research about the disease.

  • P.O. Box 700248 San Antonio, TX 78270 Phone: (210) 494-6144

Association for Glycogen Storage Disease

A parent and patient oriented support group that shares information about the disease, informs the public, and pushes for research. It also maintains a listserv to contact other members.

  • P.O. Box 896 Durant, IA 52747 Phone: (563) 785-6038

John F. And Aileen A. Crowley Foundation

A charitable foundation run by John Crowley, a Harvard Business School graduate whose quest to save his children from a rare genetic disease was the basis for the major motion picture "Extraordinary Measures".

National Institutes of Neurological Disorders and Stroke Pompe Disease Information Page

A site filled with information on Pompe Disease, maintained by the government's National Insitutues for Health.

United Pompe Foundation

An organization to raise money for Pompe disease reatment and to raise awareness of the disease.

  • c/o David W. Hamlin 5100 N. Sixth Street #119 Fresno, CA 93710 Phone: (559) 227-1898

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Clinical Trials: Pompe Disease

UF Health research scientists make medicine better every day. They discover new ways to help people by running clinical trials. When you join a clinical trial, you can get advanced medical care. Sometimes years before it's available everywhere. You can also help make medicine better for everyone else. If you'd like to learn more about clinical trials, visit our clinical trials page. Or click one of the links below:

Pompe Disease Registry

The Pompe Registry is a global, multicenter, international, longitudinal, observational, and voluntary program for patients with Pompe disease, designed to track the disease's natural history and outcomes in patients, both treated and not. Data from…

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News and Patient Stories: Pompe Disease

More Pompe Disease stories