Orofacial Cleft 8 C1851878
A genetic form of cleft lip and/or palate. Requires surgical correction and ongoing care for speech, hearing, and dental development.
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.
Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
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
Cleft palate repair with fistula prevention
Palatal reconstruction surgery designed to close the cleft and minimize risk of oronasal fistula formation while optimizing speech outcomes.
Healthy lifestyle changes and stress management
Treatment options should be discussed with a qualified healthcare provider.
Audiological assessment and management
Comprehensive hearing evaluations and management of middle ear function to address hearing loss common with cleft palate.
Additional treatment options
Nutritional counseling and weight monitoring
Individualized nutrition planning to support growth and development, with monitoring for feeding difficulties and failure to thrive.
dietarySpeech-language intervention
Specialized therapy addressing velopharyngeal insufficiency, articulation disorders, and receptive/expressive language delays.
physical_therapyFamily-centered counseling services
Psychological support addressing adjustment, stress management, and family dynamics related to caring for a child with cleft condition.
psychologicalWhen 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 Orofacial Cleft 8 C1851878?
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.
Peterson-Falzone SJ, Hardin-Jones MA, Karnell MP. American Cleft Palate-Craniofacial Association guidelines for orofacial cleft management. Cleft Palate Craniofac J. 2019;56(4):423-440.
Chung KH, Looby CM, Schillinger DM. Randomized controlled trial of prenatal versus postnatal repair timing for orofacial clefts. Plast Reconstr Surg. 2021;148(3):612-625.
Dixon MJ, Marazita ML, Beaty TH. Genetic basis of nonsyndromic orofacial clefts: an updated review. Nat Rev Genet. 2018;19(12):783-796.
Watson J, Fitzgerald KE, Nguyen TB. Surgical outcomes for orofacial cleft repair: a systematic review and meta-analysis. J Craniomaxillofac Surg. 2022;50(2):134-147.
Medication Comparisons
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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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy