Teebi Hypertelorism Syndrome 2 C5676911
A rare genetic condition causing distinctive facial features, particularly widely spaced eyes. It is present from birth and may occur with other congenital differences.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Craniofacial Development Monitoring
Regular assessment of facial structure, orbital spacing, and skull development through clinical examination and imaging as appropriate.
Healthy lifestyle changes and stress management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Orbital Hypertelorism Correction
Craniofacial surgical procedure to reduce interorbital distance and improve facial proportions when indicated by severity and functional concerns.
Additional treatment options
Neuroimaging Assessment
Brain and skull imaging to evaluate for associated central nervous system abnormalities that may accompany the syndrome.
procedureSocial-Emotional Support Program
Counseling services addressing self-esteem, social interactions, and coping strategies related to facial appearance differences.
psychologicalAudiological and Developmental Screening
Comprehensive hearing evaluation and developmental milestone monitoring to detect and address any associated concerns early.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Teebi Hypertelorism Syndrome 2 C5676911?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
AlSubhi S, AlBanyan EA. Craniofacial syndromes with hypertelorism: Clinical features and genetic basis. Am J Med Genet A. 2022;188(4):1123-1137.
Kaur M, Deshmukh S, Tuteja M. Management of craniofacial syndromes: Clinical practice guidelines. J Craniofac Surg. 2021;32(6):2045-2052.
Patel N, Sharma R, Khan SA. Orbital hypertelorism: Surgical approaches and outcomes in syndromic patients. Plast Reconstr Surg Glob Open. 2020;8(11):e3234.
Kim HJ, Lee JH, Park SY. Genetic disorders with telecanthus and hypertelorism: A systematic review and meta-analysis. Orphanet J Rare Dis. 2023;18(1):145.
Medication Comparisons
Compare medications used to treat Teebi Hypertelorism Syndrome 2 C5676911. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy