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Disorders Antibody related Hereditary Organisms Structures |
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 | Neu5Acα2 |
GM1 ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 | Neu5Acα2 |
GM1b ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide |
asialo-GM1 (GA1) | ||
GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 | Neu5Acα2 |
GM2 ganglioside | ||
GalNAcβ1-4Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 3 | | Neu5Acα2 Neu5Acα2 |
GalNAc-GD1a ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 3 | | Neu5Acα2 Neu5Acα2 |
GD1a ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 | Neu5Acα2-8Neu5Acα2 |
GD1b ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 3 | | Neu5Acα2-8Neu5Acα2 | Neu5Acα2 |
GT1a ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 3 | | Neu5Acα2 | Neu5Acα2-8Neu5Acα2 |
GT1b ganglioside | ||
Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Ceramide 3 3 | | Neu5Acα2-8Neu5Acα2 | Neu5Acα2-8Neu5Acα2 |
GQ1b ganglioside | ||
SO4-3Galβ1-1'Ceramide |
Sulfatide | ||
SO4-3GlcAβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ1-1'Ceramide |
SGPG | ||
SO4-3GlcAβ1-3Galβ1-4GlcNAcβ1-2Manα1 | 6 GlcNAcβ1-4Manβ1-4GlcNAcβ1-4GlcNAc- 3 6 | | GlcNAcβ1-2Manα1 Fucα1 |
P0 & PMP-22 oligosaccharides1 | ||
Galβ1-4GlcNAcβ1-2Man-O-Ser/Thr 3 | Neu5Acα2 |
α-Dystroglycan O-mannosylated oligosaccharides in muscle & brain | ||
| Trisulfated Heparin Disaccharide (TS-HDS) |
Microorganism | Glycolipid-like structure |
Campylobacter jejuni | GM1, GM1b, GD1a, GalNAc-GD1a GD3, GT1a, GQ1b |
Haemophilus influenzae | GM1, GT1a |
Mycoplasma pneumoniae | Galactocerebroside |
Cytomegalovirus | GM2 |
Neuropathy syndrome | Antibody target | Antibody isotype |
Chronic Sensory-Motor Demyelinating |
Myelin-associated glycoprotein (MAG) Other: SGPG, SGLPG |
IgM (monoclonal) |
Chronic ataxic neuropathy | GD1b, GD2, GD3, GT1b, GQ1b | IgM (monoclonal) |
Motor neuropathy | GM1, GalNAc-GD1a, NS6S | IgM (polyclonal or monoclonal) |
Sensory neuropathy, small fiber | TS-HDS | IgM (monoclonal) |
Sensory neuropathy | Sulfatide | IgM (monoclonal or polyclonal) |
Acute motor axonal neuropathy | GM1, GM1b, GD1a, GalNAc-GD1a | IgG |
Miller Fisher syndrome Bickerstaff’s brainstem encephalitis Acute ophthalmoparesis Ataxic Guillain–Barré syndrome |
GQ1b, GT1a | IgG |
Pharyngeal–cervical–brachial weakness | GT1a (GQ1b) | IgG |