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What is Jeune-Tommasi syndrome?

What is Jeune-Tommasi syndrome?

  • Jeune-Tommasi syndrome: A rare genetic disorder characterized by ataxia, deafness and heart problems.

Jeune-Tommasi syndrome: Introduction

Types of Jeune-Tommasi syndrome:

Broader types of Jeune-Tommasi syndrome:

Who gets Jeune-Tommasi syndrome?

Racial predominance for Jeune-Tommasi syndrome: Gypsies

How serious is Jeune-Tommasi syndrome?

Complications of Jeune-Tommasi syndrome: see complications of Jeune-Tommasi syndrome

What causes Jeune-Tommasi syndrome?

Causes of Jeune-Tommasi syndrome: see causes of Jeune-Tommasi syndrome

What are the symptoms of Jeune-Tommasi syndrome?

Symptoms of Jeune-Tommasi syndrome: see symptoms of Jeune-Tommasi syndrome

Complications of Jeune-Tommasi syndrome: see complications of Jeune-Tommasi syndrome

Can anyone else get Jeune-Tommasi syndrome?

Inheritance: see inheritance of Jeune-Tommasi syndrome

Jeune-Tommasi syndrome: Testing

Diagnostic testing: see tests for Jeune-Tommasi syndrome.

Misdiagnosis: see misdiagnosis and Jeune-Tommasi syndrome.

How is it treated?

Doctors and Medical Specialists for Jeune-Tommasi syndrome: Medical Geneticist ; see also doctors and medical specialists for Jeune-Tommasi syndrome.
Treatments for Jeune-Tommasi syndrome: see treatments for Jeune-Tommasi syndrome

Name and Aliases of Jeune-Tommasi syndrome

Main name of condition: Jeune-Tommasi syndrome

Other names or spellings for Jeune-Tommasi syndrome:

ataxia, deafness, cardiomyopathy


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