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Craniometaphyseal dysplasia, autosomal recessive type

Craniometaphyseal dysplasia, autosomal recessive type: Introduction

Craniometaphyseal dysplasia, autosomal recessive type: A rare genetic disorder characterized by head and facial abnormalities as well as mild limb abnormalities. It is a milder form of the disease than the autosomal dominant type. More detailed information about the symptoms, causes, and treatments of Craniometaphyseal dysplasia, autosomal recessive type is available below.

Symptoms of Craniometaphyseal dysplasia, autosomal recessive type

Wrongly Diagnosed with Craniometaphyseal dysplasia, autosomal recessive type?

Craniometaphyseal dysplasia, autosomal recessive type: Complications

Review possible medical complications related to Craniometaphyseal dysplasia, autosomal recessive type:

Causes of Craniometaphyseal dysplasia, autosomal recessive type

Read more about causes of Craniometaphyseal dysplasia, autosomal recessive type.

Disease Topics Related To Craniometaphyseal dysplasia, autosomal recessive type

Research the causes of these diseases that are similar to, or related to, Craniometaphyseal dysplasia, autosomal recessive type:

Craniometaphyseal dysplasia, autosomal recessive type: Broader Related Topics

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More information about Craniometaphyseal dysplasia, autosomal recessive type

  1. Craniometaphyseal dysplasia, autosomal recessive type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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