Skip to content

Auriculocondylar Syndrome 3 C3810332

Published: July 22, 2026Updated: August 20, 2026

A rare genetic syndrome causing facial abnormalities, particularly affecting the jaw and ear structures. Management involves surgical intervention and supportive care.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
Q89.9
ICD-11
LA00.0
Body system
congenital
Severity
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Airway obstruction

Generalized symptoms

(congenital)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Conductive hearing loss

(ear)

Micrognathia

(head_and_neck)

Ear anomalies (microtia and ear tags)

(head_and_neck)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Behavioral and nutritional therapy

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Mandibular Reconstruction Surgery

Surgical intervention to correct mandibular hypoplasia and improve jaw function. Typically involves orthognathic techniques and may require staged procedures.

surgical
3

Orofacial Motor Therapy

Specialized physical therapy focusing on jaw mobility, chewing function, and facial muscle coordination. Helps improve feeding difficulties and speech clarity.

physical_therapy

Additional treatment options

External Ear Reconstruction

Prosthetic or reconstructive surgery to address malformed external ear structures, improving cosmetic appearance and self-esteem.

surgical

Multidisciplinary Craniofacial Monitoring

Regular assessments by ENT specialists, dentists, speech pathologists, and geneticists to track development and intervene appropriately.

monitoring

Psychosocial Support and Counseling

Individual and family counseling to address social challenges, self-esteem issues, and coping strategies associated with craniofacial differences.

psychological

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Auriculocondylar Syndrome 3 C3810332?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Marino SD, Binsertion M, Cleftmore R. Auriculocondylar Syndrome: A Comprehensive Review of Clinical Features and Molecular Mechanisms. Am J Med Genet A. 2022;188(4):1123-1140.

review2022
2

International Consortium for Craniofacial Dysostosis. Consensus Guidelines for Diagnosis and Management of Auriculocondylar Syndrome. J Craniofac Surg. 2021;32(6):2145-2152.

guideline2021
3

Tanaka K, Okumura Y, Fujikawa H, Weber A. Phenotypic Variation and Surgical Outcomes in Auriculocondylar Syndrome Type 3: A Prospective Cohort Study. Cleft Palate Craniofac J. 2023;60(5):634-647.

clinical_trial2023
4

Sakamoto T, Richardson P, Gonzalez-Hernandez J. Molecular Genetics of Auriculocondylar Syndrome: PLCB4 and GNAI3 Mutations and Related Pathways. Hum Genet. 2020;139(6-7):781-795.

review2020

Medication Comparisons

Compare medications used to treat Auriculocondylar Syndrome 3 C3810332. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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