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Kenny-Caffey syndrome, Type 1

Kenny-Caffey syndrome, Type 1: Introduction

Kenny-Caffey syndrome, Type 1: A very rare inherited skeletal disorder involving thickening of the long bones of the body and head abnormalities. Type 1 is inherited in a recessive manner and is caused by a genetic defect located at chromosome 1q42-q43. More detailed information about the symptoms, causes, and treatments of Kenny-Caffey syndrome, Type 1 is available below.

Symptoms of Kenny-Caffey syndrome, Type 1

Wrongly Diagnosed with Kenny-Caffey syndrome, Type 1?

Kenny-Caffey syndrome, Type 1: Related Patient Stories

Kenny-Caffey syndrome, Type 1: Complications

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Causes of Kenny-Caffey syndrome, Type 1

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Disease Topics Related To Kenny-Caffey syndrome, Type 1

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Statistics for Kenny-Caffey syndrome, Type 1

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Definitions of Kenny-Caffey syndrome, Type 1:

Kenny-Caffey syndrome, Type 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Kenny-Caffey syndrome, Type 1, or a subtype of Kenny-Caffey syndrome, Type 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Kenny-Caffey syndrome, Type 1

  1. Kenny-Caffey syndrome, Type 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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