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(Top) 1 Causes 2 Diagnosis 2.1 Types 3 Treatment 4 See also 5 References 6 External links

Sulfatidosis

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Sulfatidosis
Specialty	Endocrinology

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

Causes[edit]

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

Diagnosis[edit]

Types[edit]

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

Treatment[edit]

This section is empty. You can help by adding to it. (September 2017)

References[edit]

^ "Definition: sulfatidosis from Online Medical Dictionary".

^ Sulfatidosis at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

^ 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.

External links[edit]

Lysosomal storage diseases: Inborn errorsoflipid metabolism (Lipid storage disorders)

Sphingolipidoses
(toceramide)

From ganglioside (gangliosidoses)	Ganglioside: GM1 gangliosidoses GM2 gangliosidoses (Sandhoff disease Tay–Sachs disease AB variant)
From globoside	Globotriaosylceramide: Fabry's disease
From sphingomyelin	Sphingomyelin: phospholipid: Niemann–Pick disease (SMPD1-associated type C) Glucocerebroside: Gaucher's disease
From sulfatide (sulfatidoses leukodystrophy)	Sulfatide: Metachromatic leukodystrophy Multiple sulfatase deficiency Galactocerebroside: Krabbe disease
Tosphingosine	Ceramide: Farber disease

NCL

Other

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

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