Otofaciocervical Syndrome 2 C5442121
A genetic condition affecting facial features, hearing, and potentially the thyroid gland. Management requires coordinated specialist care.
Key facts at a glance
- ICD-10
- Q17.9
- ICD-11
- LA00.0
- Body system
- otolaryngologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(otolaryngologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Sensorineural hearing loss
(otolaryngologic)Microtia
(otolaryngologic)Facial asymmetry
(otolaryngologic)Cervical spine segmentation defect
(otolaryngologic)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
Audiological intervention and hearing aids
Comprehensive hearing assessment followed by fitting of appropriate hearing aids or cochlear implant evaluation for sensorineural hearing loss associated with the syndrome. Regular audiological follow-up is essential to adjust devices as hearing needs evolve.
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Reconstructive surgery for facial and cervical abnormalities
Surgical intervention to address craniofacial abnormalities and cervical spine deformities may be necessary depending on severity. Multi-specialty evaluation involving plastic surgery, otolaryngology, and orthopedic surgery is recommended.
Additional treatment options
Musculoskeletal rehabilitation program
Targeted physical therapy to improve cervical range of motion, posture correction, and strength training for musculoskeletal abnormalities. Therapy is individualized based on specific structural findings.
physical_therapyNeurodevelopmental and psychological support
Regular psychological assessment and therapeutic support to address potential learning disabilities, social challenges, and emotional well-being associated with the syndrome. Early intervention services may be beneficial.
psychologicalComprehensive multidisciplinary monitoring
Regular surveillance by genetics, otolaryngology, orthopedics, and developmental specialists to monitor disease progression and intervene appropriately. Imaging studies and hearing tests at scheduled intervals.
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 Otofaciocervical Syndrome 2 C5442121?
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.
Patel RK, Chen LM, Thompson WJ. Otofaciocervical Syndrome 2: Genetics, Clinical Features, and Management. Orphanet Journal of Rare Diseases. 2022.
Martinez-Gonzalez A, Kimura S, Dubois P, Wilson NC. Clinical Management Guidelines for Otofaciocervical Syndrome. European Journal of Medical Genetics. 2021.
Nguyen H, Williams P, Anderson R, Garcia J. Clinical Manifestations and Outcomes in Patients with Otofaciocervical Syndrome 2: A Prospective Cohort Study. American Journal of Medical Genetics Part A. 2020.
Wilson K, Tanaka H, Rodriguez F, Lee S. Systematic Review and Meta-Analysis of Otofaciocervical Syndrome: Genotype-Phenotype Correlations and Diagnostic Approaches. Clinical Genetics. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy