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What is Megarbane-Loiselet syndrome?

What is Megarbane-Loiselet syndrome?

  • Megarbane-Loiselet syndrome: A rare syndrome characterized mainly by deafness and branchial anomalies.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Megarbane-Loiselet syndrome as a "rare disease".
Source - Orphanet

Megarbane-Loiselet syndrome: Introduction

Types of Megarbane-Loiselet syndrome:

Broader types of Megarbane-Loiselet syndrome:

What causes Megarbane-Loiselet syndrome?

Causes of Megarbane-Loiselet syndrome: see causes of Megarbane-Loiselet syndrome

What are the symptoms of Megarbane-Loiselet syndrome?

Symptoms of Megarbane-Loiselet syndrome: see symptoms of Megarbane-Loiselet syndrome

Megarbane-Loiselet syndrome: Testing

Diagnostic testing: see tests for Megarbane-Loiselet syndrome.

How is it treated?

Doctors and Medical Specialists for Megarbane-Loiselet syndrome: Otolaryngologist ; see also doctors and medical specialists for Megarbane-Loiselet syndrome.
Treatments for Megarbane-Loiselet syndrome: see treatments for Megarbane-Loiselet syndrome

Name and Aliases of Megarbane-Loiselet syndrome

Main name of condition: Megarbane-Loiselet syndrome

Other names or spellings for Megarbane-Loiselet syndrome:

Branchiogenic deafness syndrome

 

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