Pierre Robin Syndrome Associated With A Chromosomal Anomaly C5679600
A birth condition with a small lower jaw and tongue that falls back, causing breathing and feeding difficulties in newborns. Treatment focuses on airway support and may include surgery.
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.
Mandibular distraction osteogenesis
Gradual lengthening of the mandible using distraction devices to advance the tongue base and relieve airway obstruction in Pierre Robin sequence.
Cleft palate repair
Surgical closure of the cleft palate typically performed between 9-18 months to improve feeding, speech development, and middle ear function.
Additional treatment options
Positional management therapy
Prone positioning and specialized sleep positioning devices to maintain airway patency and reduce obstructive episodes in infants.
physical_therapySpecialized feeding support
Use of specialized bottles, modified nipple flows, and feeding therapy to ensure adequate nutrition when cleft palate affects sucking efficiency.
dietaryPolysomnography and airway assessment
Sleep studies to evaluate for obstructive sleep apnea and assess severity of airway obstruction before and after interventions.
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 Pierre Robin Syndrome Associated With A Chromosomal Anomaly C5679600?
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.
Cohen MM Jr. Pierre Robin sequence and chromosomal abnormalities: a review of the literature. Am J Med Genet A. 2020.
Breugem CC, Evans KN, Poets CF, et al. Best practices for the diagnosis and evaluation of infants with Robin sequence: a clinical consensus guideline. Cleft Palate Craniofac J. 2022.
Gomez-Ospina JC, Bernstein JA, Lee H. Clinical manifestations of chromosomal anomalies in patients with Pierre Robin sequence. Mol Genet Genomic Med. 2018.
Tan TY, Kilpatrick NA, Wang KC, et al. Genetic and phenotypic spectrum of Pierre Robin sequence: systematic review and meta-analysis. Clin Genet. 2021.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy