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Ectodermal dysplasia -- alopecia -- preaxial polydactyly

Ectodermal dysplasia -- alopecia -- preaxial polydactyly: Introduction

Ectodermal dysplasia -- alopecia -- preaxial polydactyly: A rare syndrome characterized by facial abnormalities, extra toes and sparse or absent hair. More detailed information about the symptoms, causes, and treatments of Ectodermal dysplasia -- alopecia -- preaxial polydactyly is available below.

Symptoms of Ectodermal dysplasia -- alopecia -- preaxial polydactyly

Wrongly Diagnosed with Ectodermal dysplasia -- alopecia -- preaxial polydactyly?

Ectodermal dysplasia -- alopecia -- preaxial polydactyly: Related Patient Stories

Causes of Ectodermal dysplasia -- alopecia -- preaxial polydactyly

Read more about causes of Ectodermal dysplasia -- alopecia -- preaxial polydactyly.

Misdiagnosis and Ectodermal dysplasia -- alopecia -- preaxial polydactyly

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Ectodermal dysplasia -- alopecia -- preaxial polydactyly: Animations

Statistics for Ectodermal dysplasia -- alopecia -- preaxial polydactyly

Ectodermal dysplasia -- alopecia -- preaxial polydactyly: Broader Related Topics

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Definitions of Ectodermal dysplasia -- alopecia -- preaxial polydactyly:

Ectodermal dysplasia -- alopecia -- preaxial polydactyly is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Ectodermal dysplasia -- alopecia -- preaxial polydactyly, or a subtype of Ectodermal dysplasia -- alopecia -- preaxial polydactyly, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

 

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