Hypotelorism

Hypotelorism is a medical condition characterized by a decreased distance between two organs or bodily features. In the context of craniofacial abnormalities, hypotelorism refers to the reduced distance between the eyes or orbits. This condition is often associated with various genetic disorders and syndromes.

Causes[edit | edit source]

Hypotelorism is often a symptom of a broader genetic disorder or syndrome. It can be associated with conditions such as Holoprosencephaly, a disorder characterized by the failure of the forebrain to develop properly, and Smith-Lemli-Opitz syndrome, a developmental disorder that affects multiple parts of the body.

Diagnosis[edit | edit source]

Diagnosis of hypotelorism is typically made through a physical examination and imaging studies such as CT scans or MRI. Genetic testing may also be performed to identify any underlying genetic disorders or syndromes.

Treatment[edit | edit source]

Treatment for hypotelorism is typically focused on managing the underlying condition and improving the individual's quality of life. This may involve surgery to correct the positioning of the eyes or orbits, or other treatments as appropriate for the underlying condition.