• Source: Gangliosidosis

Gangliosidosis contains different types of lipid storage disorders 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




See also


Sphingolipidoses#Overview




References






External links

Kata Kunci Pencarian:

• ICD-10 Bab IV: Penyakit endokrin, nutrisi, dan metabolik
• Saposin
• Hepatosplenomegali
• Penyakit Tay-Sachs
• Mukolipidosis
• Beta-galaktosidase
• Gangliosidosis
• Tay–Sachs disease
• GM1 gangliosidoses
• GM2 gangliosidoses
• List of diseases (G)
• Sandhoff disease
• Lysosomal storage disease
• GM 2 gangliosidosis
• Ganglioside
• Korat