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Brachytelephalangy, characteristic facies, Kallmann

Brachytelephalangy, characteristic facies, Kallmann: Introduction

Brachytelephalangy, characteristic facies, Kallmann: A very rare syndrome characterized primarily by very short end bones of fingers and facial anomalies. More detailed information about the symptoms, causes, and treatments of Brachytelephalangy, characteristic facies, Kallmann is available below.

Symptoms of Brachytelephalangy, characteristic facies, Kallmann

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Definitions of Brachytelephalangy, characteristic facies, Kallmann:

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

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More information about Brachytelephalangy, characteristic facies, Kallmann

  1. Brachytelephalangy, characteristic facies, Kallmann: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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