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Pyknoachondrogenesis

Pyknoachondrogenesis: Introduction

Pyknoachondrogenesis: A very rare lethal syndrome characterized mainly by abnormal skeletal growth as well as abnormal bone calcification. More detailed information about the symptoms, causes, and treatments of Pyknoachondrogenesis is available below.

Symptoms of Pyknoachondrogenesis

Wrongly Diagnosed with Pyknoachondrogenesis?

Pyknoachondrogenesis: Related Patient Stories

Pyknoachondrogenesis: Complications

Review possible medical complications related to Pyknoachondrogenesis:

Causes of Pyknoachondrogenesis

Read more about causes of Pyknoachondrogenesis.

Statistics for Pyknoachondrogenesis

Pyknoachondrogenesis: Broader Related Topics

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Definitions of Pyknoachondrogenesis:

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

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More information about Pyknoachondrogenesis

  1. Pyknoachondrogenesis: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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