Cleft of Chin

Understanding face related symptoms and features.

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 face contains the nose, eyes and mouth, all of which are sensory organs. The face also displays emotions and feelings and plays a crucial role in communication. The face runs from the forehead at the top, to the chin at the bottom and encompasses everything in between.

Symptoms affecting the face can for the most part be seen with the naked eye. Although diagnosing a face related symptom may involve different tests and assessments, both subjective and objective.

Symptoms relating to the face may affect its structure, shape and/ or function. Some features will affect just the appearance of the face while others may affect its ability to express emotions and to communicate non-verbally.

What is the Cleft of chin?

Cleft of chin refers to a developmental or growth defect which causes the chin to not fuse together properly. This then creates a cleft, line or fissure as it may be referred to through the middle or midline of the chin.

Generally cleft of the chin occurs before birth, and as the fetus is developing, the two parts of the chin fail to fuse together.

What should I do next?

In some instances, the cleft of chin may be one of the features of a rare disease or genetic syndrome. In this case fast, targeted genetic analysis can give you a more accurate diagnosis.

FDNA™ Health can help you with the diagnostic journey.

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