Neuromuscular HOMEepAGE
neuromuscular.wustl.edu
/
A–Z

Sensory Neuronopathies

MitochondrialImmune/Antibody
W
View full entry on WUSTL Neuromuscular
antibody/sneuron.html#Sensory Neuronopathies 14

Overview

From WUSTL Neuromuscular

Immune Paraneoplastic with anti-Hu antibodies Sjögren's syndrome Acute: Sensory neuronopathy IgG vs FGFR3 IgG vs Amphiphysin IgM vs TS-HDS Small fiber neuropathy: Non-length dependent Idiopathic Pan-sensory Small fiber Drugs Pyridoxine intoxication Acute High dose (100 - 200 g) Neuronopathy Chronic Moderate dose (0.2 - 10 g/day) Distal axonopathy, Reversible cis-platinum Doxorubicin Animals only: No human cases described Hereditary HSN CANVAS: RFC1 Mitochondrial COX20 POLG HADHA Friedreich Ataxia: Frataxin SCO2 SNAX1 SCA4 SCA25 AVED: ATTP Localized Herpes zoster Also see Sensory Ataxia Dorsal

Related Conditions

Shared genes
Axonal Sensory Neuropathies with Serum IgM binding to Trisulfated Heparin Disaccharide (TS-HDS)
HDSDISACCHARIDEMAG
CHRONIC IMMUNE POLYNEUROPATHIES: AXONAL
HDS
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A (FSHMD 1A)
DNMT3BLRIF1SMALL
Monoclonal Gammopathies of Unknown Significance (& Other)
MAGGD1AHDS
Neuropathy with IgM binding to Myelin-Associated Glycoprotein (MAG)
MAGHDSPHOSPHACAN
Other Muscle Features
VAMPINCLUSIONBCIM
Rituximab Infusion Protocol
GD1AHDS
Specific associated clinical syndromes
GD1AHDSTUBULIN

External Resources

WUSTL Neuromuscular
Washington University Disease Center
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.