Gangliosidosis

Gangliosidosis
Classification and external resources
Specialty	endocrinology
ICD-10	E75.0-E75.1
ICD-9-CM	330.1
MeSH	D005733
Orphanet	309144

Gangliosidosis contains different types of lipid storage disorders^[1] caused by the accumulation of lipids known as gangliosides. There are two distinct genetic causes of the disease. Both are autosomal recessive and affect males and females equally.

Types

GM1 gangliosidoses - GM1
GM2 gangliosidoses - GM2

References

↑ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 1437709494.

External links

Hide & Seek Foundation for Lysosomal Disease Research

(LSD) Inborn error of lipid metabolism: lipid storage disorders (E75, 272.7–272.8)

Sphingolipidoses
(to ceramide)

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
To sphingosine	Ceramide: Farber disease

NCL

Other

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Gangliosidosis

Types

See also

References

External links