Structured Summary
Abstract
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).
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1 entry terms
- Sulfatidoses
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34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2007; use LEUKODYSTROPHY, METACHROMATIC 1974-2006
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References
- National Library of Medicine. Sulfatidosis. Medical Subject Headings (MeSH). 2026. Unique ID D052516. http://id.nlm.nih.gov/mesh/2026/D052516
- Sulfatidosis. In: Wikipedia. https://en.wikipedia.org/wiki/Sulfatidosis
- Sulfatidosis. In: Wikidata. https://www.wikidata.org/wiki/Q7636192