Pompe Disease Causes, Symptoms and Treatment and Related Disorders
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Pompe Disease
National Organization for Rare Disorders, Inc.
Synonyms ...
NINDS Pompe Disease Information Page
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What is Pompe disease?
Pompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body's cells.
Acid Maltase Deficiency (Pompe Disease) - Support Group
Acid Maltase Deficiency Association (AMDA) - Support Group
Acid Maltase Deficiency Association (AMDA) - Acid Maltase Deficiency (Pompe Disease) - Support Group ...
The infantile form of Pompe disease starts before the age of 3 months with major hypotonia, sucking and swallowing difficulties, hypertrophic cardiomyopathy and progressive hepatomegaly.
Acid Maltase Deficiency see Pompe disease
Acne
Acne Vulgaris see Acne
Acoustic Neuroma
Acquired Aplastic Anaemia
Acquired Aplastic Anemia see Acquired Aplastic Anaemia
Acquired Haemochromatosis see Haemochromatosis ...
Acid maltase deficiency (AMD), also known as Pompe disease, is a genetically inherited disease that affects muscle function. Inherited diseases are passed on from parents to a child.
Acid maltase deficiency, also called Pompe disease, is a non-sex linked recessive genetic disorder that is the most serious of the glycogen storage diseases affecting muscle tissue.
Pompe disease ... Lower back pain
Porphyria ... back pain
Post streptococcal glomerulonephritis ... dull back pain
Pregnancy-associated osteoporosis ... back pain
Prostate Cancer ... lower back pain
Prostate cancer, familial ... back pain ...
» Genzyme Receives FDA Approval for Lumizyme for Pompe Disease
» Genzyme Corp. Signs Consent Decree to Correct Violations at Allston, Mass., Manufacturing Plant and Give up $175 Million in Profits ...
Maroteaux-Larny disease-affects the skin, bones, liver, and spleen
Niemann-Pick disease-affects the spleen, liver, and lungs
Pompe disease-affects the liver, heart, and muscle tissue
Tay-Sachs disease-affects the brain ...
[abstract]
Kishnani PS, Hwu WL, Mandel H, et al; A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr. 2006 May;148(5):671-676. [abstract] ...
 See also: Deficiency, Storage disease, Glycogen Storage Disease, Symptom, Sclerosis
  
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