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Catel-Manzke Syndrome



Catel-Manzke Syndrome: Introduction

Catel-Manzke Syndrome: A rare genetic disorder characterized by a small jaw, cleft palate and an extra bone at the base of the pointer finger. More detailed information about the symptoms, causes, and treatments of Catel-Manzke Syndrome is available below.

Symptoms of Catel-Manzke Syndrome

See full list of 12 symptoms of Catel-Manzke Syndrome

Catel-Manzke Syndrome: Complications

Review possible medical complications related to Catel-Manzke Syndrome:

Less Common Symptoms of Catel-Manzke Syndrome

See full list of 17 occasional symptoms of Catel-Manzke Syndrome

Wrongly Diagnosed with Catel-Manzke Syndrome?

Causes of Catel-Manzke Syndrome

Read more about causes of Catel-Manzke Syndrome.

More information about causes of Catel-Manzke Syndrome:

Evidence Based Medicine Research for Catel-Manzke Syndrome

Medical research articles related to Catel-Manzke Syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Videos for Catel-Manzke Syndrome

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Reseach about Catel-Manzke Syndrome

Visit our research pages for current research about Catel-Manzke Syndrome treatments.

Stories from Users Related to Catel-Manzke Syndrome

User Interactive Forums

Read about other experiences, ask a question about Catel-Manzke Syndrome, or answer someone else's question, on our message boards:

Definitions of Catel-Manzke Syndrome:

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


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