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Cushing's symphalangism

Cushing's symphalangism: Introduction

Cushing's symphalangism: A rare syndrome characterized by deafness and the fusion of joints in the middle of fingers and toes as well as fusion of hand and foot bones. More detailed information about the symptoms, causes, and treatments of Cushing's symphalangism is available below.

Symptoms of Cushing's symphalangism

Home Diagnostic Testing

Home medical testing related to Cushing's symphalangism:

Wrongly Diagnosed with Cushing's symphalangism?

Cushing's symphalangism: Related Patient Stories

Cushing's symphalangism: Complications

Read more about complications of Cushing's symphalangism.

Causes of Cushing's symphalangism

Read more about causes of Cushing's symphalangism.

Disease Topics Related To Cushing's symphalangism

Research the causes of these diseases that are similar to, or related to, Cushing's symphalangism:

Misdiagnosis and Cushing's symphalangism

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Cushing's symphalangism: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Cushing's symphalangism: Animations

Statistics for Cushing's symphalangism

Cushing's symphalangism: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Cushing's symphalangism, or answer someone else's question, on our message boards:

Definitions of Cushing's symphalangism:

Cushing's symphalangism is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Cushing's symphalangism, or a subtype of Cushing's symphalangism, 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 Cushing's symphalangism as a "rare disease".
Source - Orphanet

 

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