Usher syndrome, type 1E

Common Name(s)

Usher syndrome, type 1E

Usher syndrome is a genetic condition characterized by hearing loss or deafness, and progressive vision loss due to retinitis pigmentosa. Three major types of Usher syndrome have been described - types I, II, and III.  The different types are distinguished by their severity and the age when signs and symptoms appear. All three types are inherited in an autosomal recessive manner, which means both copies of the disease-causing gene in each cell have mutations.
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Advocacy and Support Organizations Health Questions Recommended Apps Scientific Literature Symptoms, Diagnosis, and Treatment Clinical Trial Information
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Usher syndrome, type 1E" for support, advocacy or research.

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General Support Organizations

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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 "Usher syndrome, type 1E" 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

 
 
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Recommended Apps

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.

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Relief is when you and the right researcher find each other

Finding the right clinical trial for Usher syndrome, type 1E can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.

Learn More
 
 
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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 "Usher syndrome, type 1E" returned 0 free, full-text research articles on human participants.

No free, full-text research articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Usher syndrome, type 1E".

Reviews from the PubMed Database

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

No free, full-text review articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Usher syndrome, type 1E".

 
 
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Symptoms, Diagnosis, and Treatment

This information is provided by Genetics Home Reference.
https://ghr.nlm.nih.gov/condition/usher-syndrome
https://ghr.nlm.nih.gov/gene/CLRN1
https://ghr.nlm.nih.gov/gene/PDZD7
https://ghr.nlm.nih.gov/gene/USH1C
https://ghr.nlm.nih.gov/gene/USH2A
https://ghr.nlm.nih.gov/gene/USH1G
https://ghr.nlm.nih.gov/gene/EML1
https://ghr.nlm.nih.gov/gene/GPR179
https://ghr.nlm.nih.gov/gene/CDH23
https://ghr.nlm.nih.gov/gene/MYO7A
https://ghr.nlm.nih.gov/gene/PCDH15
https://ghr.nlm.nih.gov/gene/WHRN
https://ghr.nlm.nih.gov/gene/ADGRV1
https://ghr.nlm.nih.gov/gene/CIB2
https://ghr.nlm.nih.gov/condition/otopalatodigital-syndrome-type-1
https://ghr.nlm.nih.gov/condition/otopalatodigital-syndrome-type-2
https://ghr.nlm.nih.gov/gene/CEP78
https://ghr.nlm.nih.gov/condition/trichorhinophalangeal-syndrome-type-ii
https://ghr.nlm.nih.gov/condition/distal-arthrogryposis-type-1
https://ghr.nlm.nih.gov/condition/mucopolysaccharidosis-type-i
Full Results at Genetics Home Reference: 2916 matches

There are currently no related results available in GeneReviews.

This information is provided by Genetic Testing Registry.
http://www.ncbi.nlm.nih.gov/gtr/conditions/C1865865
 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.

According to ClinicalTrials.gov there are currently 0 additional "open" studies for "Usher syndrome, type 1E" (open studies are recruiting volunteers) and 0 "Usher syndrome, type 1E" studies with "all" status. Visit ClinicalTrials.gov now to view them. Or alternatively, consider TrialsFinder for assistance:
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Relief is when you and the right researcher find each other
Finding the right clinical trial for Usher syndrome, type 1E can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
Learn More