Sarcoglycanopathies

Overview

Deficiencies or mutations in the genes for the SARCOGLYCAN COMPLEX subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.

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 Sarcoglycanopathies

Topic type

Condition

Category

Cardiology

MeSH classification

C05.651.534.500.280.500|C08.618.923|C10.668.491.175.500.149.500|C14.280.238.812|C16.320.577.280.500

Preparing for an appointment about Sarcoglycanopathies

If you are speaking with a healthcare professional about Sarcoglycanopathies, 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.

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