Hypotelorism

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
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Hypotelorism
File:Hypotelorism.png
Synonyms
Pronounce	N/A
Specialty	N/A
Symptoms	Decreased distance between the eyes
Complications
Onset	Congenital
Duration	Lifelong
Types	N/A
Causes	Genetic disorders, chromosomal abnormalities
Risks
Diagnosis	Physical examination, imaging studies
Differential diagnosis	Hypertelorism, craniosynostosis
Prevention
Treatment	Surgical intervention
Medication
Prognosis	Depends on underlying cause
Frequency	Rare
Deaths	N/A

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

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

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

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.

See also

• Hypertelorism
• Telecanthus