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Diseases » Usher Syndrome 1H » Summary

What is Usher Syndrome 1H?

What is Usher Syndrome 1H?

  • Usher Syndrome 1H: A rare inherited disorder characterized by sensorineural deafness and progressive vision loss which starts during the first decade of life and blindness usually occurs between 20-35 years of age. Symptoms are generally more severe than in type 2 with deafness occurring at birth or during first year and vision loss starting during childhood. The defect occurs on chromosome 17q24-q25.

Usher Syndrome 1H: Introduction

Types of Usher Syndrome 1H:

Broader types of Usher Syndrome 1H:

What causes Usher Syndrome 1H?

Causes of Usher Syndrome 1H: see causes of Usher Syndrome 1H

What are the symptoms of Usher Syndrome 1H?

Symptoms of Usher Syndrome 1H: see symptoms of Usher Syndrome 1H

Onset of Usher Syndrome 1H: Deafness was present from birth and vision problems occurred with increasing age.

Usher Syndrome 1H: Testing

Diagnostic testing: see tests for Usher Syndrome 1H.

Misdiagnosis: see misdiagnosis and Usher Syndrome 1H.

How is it treated?

Treatments for Usher Syndrome 1H: see treatments for Usher Syndrome 1H

Name and Aliases of Usher Syndrome 1H

Main name of condition: Usher Syndrome 1H

Other names or spellings for Usher Syndrome 1H:

Usher Syndrome type 1H


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