Orofacial Cleft 4 C1842143
A birth condition where tissues of the lip or palate do not join completely. Surgical reconstruction and rehabilitation help restore function and appearance.
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
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Primary Cleft Lip and Alveolar Repair
Combined surgical repair of lip and alveolar ridge (gum line) typically performed in early infancy to restore appearance and enable proper tooth development.
Nutritional Support and Monitoring
Comprehensive nutritional assessment and support ensuring adequate caloric intake and proper weight gain during early infancy when feeding challenges exist.
Additional treatment options
Nasal Alveolar Molding (NAM)
Pre-surgical nasoalveolar molding uses custom oral appliances to gradually reshape gum, lip, and nasal tissues for improved surgical outcomes.
procedureHearing and Ear Tube Surveillance
Regular audiological assessments and potential pressure equalization (PE) tube placement to manage middle ear fluid and prevent hearing loss associated with cleft palate.
monitoringDental and Orthodontic Intervention
Comprehensive orthodontic care including primary tooth management, palate expansion, and alignment correction throughout childhood and adolescence.
complementaryWhen 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 4 C1842143?
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.
American Cleft Palate Association. Parameters for evaluation and treatment of patients with cleft lip/palate or other craniofacial anomalies. Cleft Palate Craniofac J. 2020.
Rattanasiri S, Boonprakong K, Auychai P. Meta-analysis of IRF6 gene variants and nonsyndromic orofacial clefting. Hum Genet. 2022.
Wang L, Chen H, Zhang J, Liu Y. Surgical outcomes of early versus delayed palate repair in cleft patients: a prospective cohort study. Plast Reconstr Surg. 2018.
Natsume N, Kawai T, Imaizumi K, Tanaka R. Genetic and environmental factors in orofacial cleft malformations: a comprehensive review. J Oral Maxillofac Surg. 2016.
Medication Comparisons
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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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy