Craniodiaphyseal dysplasia

Craniodiaphyseal dysplasia (also known as CDD or Lionitis) is a rare, severe bone disorder that primarily affects the skull and facial bones. The condition is characterized by abnormal bone growth, leading to a variety of symptoms and complications.

Symptoms

The most common symptoms of craniodiaphyseal dysplasia include:

• Facial deformity
• Hearing loss
• Vision problems
• Breathing difficulties
• Headache
• Seizures

Causes

Craniodiaphyseal dysplasia is caused by mutations in the ANO5 gene. This gene provides instructions for making a protein that is involved in the regulation of bone growth. Mutations in the ANO5 gene disrupt this regulation, leading to the abnormal bone growth seen in craniodiaphyseal dysplasia.

Diagnosis

Diagnosis of craniodiaphyseal dysplasia is typically based on the characteristic physical features and confirmed by genetic testing for mutations in the ANO5 gene.

Treatment

There is currently no cure for craniodiaphyseal dysplasia. Treatment is focused on managing symptoms and improving quality of life. This may include surgery to improve breathing or vision, physical therapy to improve mobility, and medication to manage pain and other symptoms.

Prognosis

The prognosis for individuals with craniodiaphyseal dysplasia varies. Some individuals may have a normal lifespan with manageable symptoms, while others may experience severe complications that can be life-threatening.

See also

• Bone disorder
• Genetic disorder
• Rare disease

References

Craniodiaphyseal dysplasia Resources
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