Condition
Glycogen Storage Disease Type IIb
Cardiology
Overview
An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Glycogen Storage Disease Type IIb
- Topic type
- Condition
- Category
- Cardiology
- MeSH classification
- C10.597.606.360.455.562|C14.280.238.458|C16.320.322.201|C16.320.565.202.449.510|C18.452.648.202.449.510
Preparing for an appointment about Glycogen Storage Disease Type IIb
If you are speaking with a healthcare professional about Glycogen Storage Disease Type IIb, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
Finding care related to Glycogen Storage Disease Type IIb
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.