Sensory neuropathy type 1

Common Name(s)

Sensory neuropathy type 1

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Sensory neuropathy type 1" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

Not finding the support you need? Show General Support Organizations

 
 
Top

How do you compare to others with this condition?

Privately answer questions about your health. Let resources, you select, come to you.

Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.

 
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Sensory neuropathy type 1" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

Not finding the support you need? Show General Support Organizations

 
 
 
 
Top

Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Sensory neuropathy type 1" returned 10 free, full-text research articles on human participants. First 3 results:

Natural history and biomarkers in hereditary sensory neuropathy type 1.
 

Author(s): Vera Fridman, Anne Louise Oaklander, William S David, Elise A Johnson, Jessica Pan, Peter Novak, Robert H Brown, Florian S Eichler

Journal: Muscle Nerve. 2015 Apr;51(4):489-95.

 

Hereditary sensory and autonomic neuropathy type 1 (HSAN1) is most commonly caused by missense mutations in SPTLC1. In this study we mapped symptom progression and compared the utility of outcomes.

Last Updated: 20 Mar 2015

Go To URL
Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2.
 

Author(s): Sinéad M Murphy, Daniela Ernst, Yu Wei, Matilde Laurà, Yo-Tsen Liu, James Polke, Julian Blake, John Winer, Henry Houlden, Thorsten Hornemann, Mary M Reilly

Journal: Neurology. 2013 Jun;80(23):2106-11.

 

To describe the clinical and neurophysiologic phenotype of a family with hereditary sensory and autonomic neuropathy type 1 (HSANI) due to a novel mutation in SPTLC2 and to characterize the biochemical properties of this mutation.

Last Updated: 4 Jun 2013

Go To URL
Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1.
 

Author(s): Kevin Garofalo, Anke Penno, Brian P Schmidt, Ho-Joon Lee, Matthew P Frosch, Arnold von Eckardstein, Robert H Brown, Thorsten Hornemann, Florian S Eichler

Journal: J. Clin. Invest.. 2011 Dec;121(12):4735-45.

 

Hereditary sensory and autonomic neuropathy type 1 (HSAN1) causes sensory loss that predominantly affects the lower limbs, often preceded by hyperpathia and spontaneous shooting or lancinating pain. It is caused by several missense mutations in the genes encoding 2 of the 3 subunits ...

Last Updated: 11 Jan 2012

Go To URL

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Sensory neuropathy type 1" returned 0 free, full-text review articles on human participants.

 
 
Top

Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

There are currently no related results available in Genetic Testing Registry.

 
 
Top

Clinical Trial Information This information is provided by ClinicalTrials.gov

Assessing Long Term Safety and Tolerability of PXT3003 in Patients With Charcot-Marie-Tooth Disease Type 1A
 

Status: Not yet recruiting

Condition Summary: Charcot-Marie-Tooth Disease, Type IA

 

Last Updated: 13 Jan 2017

Go to URL
Tools for Therapeutic Evaluation in Charcot-Marie-Tooth Disease Type 1A: Outcome Measures and Biomarkers
 

Status: Not yet recruiting

Condition Summary: Charcot-Marie-Tooth Disease Type 1A

 

Last Updated: 3 Nov 2015

Go to URL
SERENDEM : MD1003 in Patients Suffering From Demyelinating Neuropathies, an Open Label Pilot Study
 

Status: Recruiting

Condition Summary: Chronic Inflammatory Demyelinating Polyneuropathy; Peripheral Neuropathy; Charcot-Marie-Tooth Disease; Charcot-Marie-Tooth Disease Type 1A; Charcot-Marie-Tooth Disease, Type IA

 

Last Updated: 15 Nov 2016

Go to URL