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What is Epiphyseal dysplasia dysmorphism camptodactyly?

What is Epiphyseal dysplasia dysmorphism camptodactyly?

  • Epiphyseal dysplasia dysmorphism camptodactyly: A rare syndrome characterized mainly by hearing loss, unusual face and bone development abnormalities.

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

Epiphyseal dysplasia dysmorphism camptodactyly: Introduction

Types of Epiphyseal dysplasia dysmorphism camptodactyly:

Broader types of Epiphyseal dysplasia dysmorphism camptodactyly:

What causes Epiphyseal dysplasia dysmorphism camptodactyly?

Causes of Epiphyseal dysplasia dysmorphism camptodactyly: see causes of Epiphyseal dysplasia dysmorphism camptodactyly

What are the symptoms of Epiphyseal dysplasia dysmorphism camptodactyly?

Symptoms of Epiphyseal dysplasia dysmorphism camptodactyly: see symptoms of Epiphyseal dysplasia dysmorphism camptodactyly

Epiphyseal dysplasia dysmorphism camptodactyly: Testing

Diagnostic testing: see tests for Epiphyseal dysplasia dysmorphism camptodactyly.

How is it treated?

Treatments for Epiphyseal dysplasia dysmorphism camptodactyly: see treatments for Epiphyseal dysplasia dysmorphism camptodactyly

Name of Epiphyseal dysplasia dysmorphism camptodactyly

Main name of condition: Epiphyseal dysplasia dysmorphism camptodactyly

 

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