Sulfatidosis

Medical condition
Sulfatidosis
SpecialtyEndocrinology

Sulfatidosis is a form of lysosomal storage disease resulting in a proliferation of sulfatide.

Causes

It is caused by a genetic insufficiency of sulfatase enzymes.[1]

Diagnosis

Types

Metachromatic leukodystrophy and multiple sulfatase deficiency are classified as sulfatidoses.[2][3]

Treatment

See also

  • Sphingolipidoses#Overview for an overview table, including sulfatidosis

References

  1. ^ "Definition: sulfatidosis from Online Medical Dictionary".
  2. ^ Sulfatidosis at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  3. ^ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease. St. Louis, Mo: Elsevier Saunders. p. 161. ISBN 978-0-7216-0187-8.
Classification
D
  • MeSH: D052516
  • v
  • t
  • e
Lysosomal storage diseases: Inborn errors of lipid metabolism (Lipid storage disorders)
Sphingolipidoses
(to ceramide)
From ganglioside
(gangliosidoses)
From globoside
From sphingomyelin
From sulfatide
(sulfatidoses
To sphingosine
NCL
Other


Stub icon

This article about an endocrine, nutritional, or metabolic disease is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e