Sulfatidosis

Overview

A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH of the brain. These disorders are caused by defective degradative enzymes leading to substrate accumulation (or storage).

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 Sulfatidosis

Topic type

Condition

Category

Neurology

MeSH classification

C10.228.140.163.100.435.825.850|C16.320.565.189.435.825.850|C16.320.565.398.641.803.925|C16.320.565.595.554.825.850|C18.452.132.100.435.825.850|C18.452.584.563.641.803.925|C18.452.648.189.435.825.850|C18.452.648.398.641.803.925|C18.452.648.595.554.825.850

Preparing for an appointment about Sulfatidosis

If you are speaking with a healthcare professional about Sulfatidosis, 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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