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Hay-Wells syndrome, recessive type

Hay-Wells syndrome, recessive type: Introduction

Hay-Wells syndrome, recessive type: A rare recessively inherited genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. The recessive form of this condition is distinguished by the presence at birth of adhesions between the upper and lower jaws. More detailed information about the symptoms, causes, and treatments of Hay-Wells syndrome, recessive type is available below.

Symptoms of Hay-Wells syndrome, recessive type

Home Diagnostic Testing

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Wrongly Diagnosed with Hay-Wells syndrome, recessive type?

Hay-Wells syndrome, recessive type: Related Patient Stories

Hay-Wells syndrome, recessive type: Complications

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Causes of Hay-Wells syndrome, recessive type

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Disease Topics Related To Hay-Wells syndrome, recessive type

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Hay-Wells syndrome, recessive type: Undiagnosed Conditions

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Misdiagnosis and Hay-Wells syndrome, recessive type

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Hay-Wells syndrome, recessive type: Research Doctors & Specialists

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Hospitals & Clinics: Hay-Wells syndrome, recessive type

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Hay-Wells syndrome, recessive type: Animations

Statistics for Hay-Wells syndrome, recessive type

Hay-Wells syndrome, recessive type: Broader Related Topics

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Definitions of Hay-Wells syndrome, recessive type:

Hay-Wells syndrome, recessive type is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Hay-Wells syndrome, recessive type, or a subtype of Hay-Wells syndrome, recessive type, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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