Acid Maltase Deficiency Disease, also known as Pompe disease, is a rare genetic disorder. The word "acid" is pronounced as /ˈæsɪd/ while "maltase" is pronounced as /ˈmɔːlteɪs/. The word "deficiency" is pronounced as /dɪˈfɪʃənsi/. Altogether, the word is spelled as /ˈæsɪd ˈmɔːlteɪs dɪˈfɪʃənsi dɪˈziːz/. The disease is caused by the deficiency of an enzyme called acid alpha-glucosidase, leading to the accumulation of glycogen in muscles and tissues. Symptoms include muscle weakness and respiratory difficulties.
Acid Maltase Deficiency Disease, also known as Pompe Disease, is a rare inherited metabolic disorder characterized by the deficiency or absence of the enzyme alpha-glucosidase, also called acid maltase. This enzyme is responsible for breaking down glycogen, a complex sugar that serves as a stored source of energy in cells, into glucose, which can be readily used by the body.
Due to the deficiency of acid maltase, glycogen accumulates in various tissues, particularly muscle tissues. This excessive buildup leads to progressive muscle weakness and wasting, as well as impaired function of other organs, such as the heart and respiratory system.
The symptoms and severity of Acid Maltase Deficiency Disease can vary widely. In more severe cases, infants may present with weak muscle tone, difficulties in feeding and breathing, and a failure to thrive. In less severe cases, the signs and symptoms may appear later in childhood or even adulthood, typically manifesting as muscle weakness, fatigue, respiratory problems, and mobility impairments.
Currently, there is no cure for Acid Maltase Deficiency Disease, and treatment is primarily focused on managing the symptoms and improving the individual's quality of life. This may involve a multidisciplinary approach, including the administration of enzyme replacement therapy to supplement the deficient enzyme, physical therapy to improve muscle strength and mobility, respiratory support, and other supportive measures.
Overall, Acid Maltase Deficiency Disease is a rare genetic disorder that affects the body's ability to break down glycogen, leading to progressive muscle weakness and impairments in various organ systems.