Craniofacial Asymmetry

What is Craniofacial Asymmetry?

Craniofacial Asymmetry affects the bones of the face and the skull. It refers to when both are asymmetric. They may be malformed or uneven.

Symptoms may affect multiple parts of the body. Understanding which part of the body a symptom affects, can help us to better understand the potential underlying causes of a symptom, including a rare disease or genetic syndrome.

The skull has several crucial functions: it cradles and protects the brain, supports the face and forms the head. It is a bony structure made up of the mandible and cranium.

Symptoms affecting the skull can sometimes be seen with the naked eye, especially if they affect the shape, size, and structure of the head and face. Diagnosing a skull-related symptom may involve different tests and assessments, both subjective and objective.

This condition can result in functional issues such as difficulty with breathing, chewing, or speaking, depending on the severity of the asymmetry and which areas are affected.

What should I do next?

In some instances, craniofacial asymmetry may be one of the features of a rare disease or genetic syndrome. To find out if someone with Craniofacial Asymmetry, may be due to a genetic syndrome, it is important to have a consultation and evaluation with a clinical genetic specialist.  Specialists may also suggest specific genetic testing or other types of tests to help reach a diagnosis.  FDNA’s AI technology can help speed up the diagnostic process by analyzing facial features and other health information.

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