 | This article needs editing to comply with Wikipedia's
Manual of Style. In particular, it has problems with not using MEDMOS. (July 2017) |
| Gangliosidosis | |
|---|---|
| Specialty |
Endocrinology
 |
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
See also
References
- ^ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 978-1437709490.
External links
| Authority control databases: National |
|---|
 | This article about an endocrine, nutritional, or metabolic disease is a stub. You can help Wikipedia by expanding it. |
| This article needs editing to comply with Wikipedia's
Manual of Style. In particular, it has problems with not using MEDMOS. (July 2017) |
| Gangliosidosis | |
|---|---|
| Specialty |
Endocrinology
|
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
See also
References
- ^ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 978-1437709490.
External links
| Authority control databases: National |
|---|
|
| This article about an endocrine, nutritional, or metabolic disease is a stub. You can help Wikipedia by expanding it. |