Research Evidence
Peer-reviewed studies linked via MeSH term "Pierre Robin Syndrome" from the MEDLINE/PubMed database.
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Genetic Landscape of Robin Sequence: A Systematic Review.
[object Object], [object Object], [object Object] et al. · Clin Genet · 2026
Characterizing Differences in Polysomnography Data for Children With Robin Sequence Undergoing Conservative and Surgical Management.
[object Object], [object Object], [object Object] et al. · Otolaryngol Head Neck Surg · 2025
Robin Sequence: From Dilemmas to Developing an Adaptable Standardized Stepwise Approach.
[object Object], [object Object], [object Object] et al. · Acta Paediatr · 2025
Neurodevelopmental impairment in children with Robin sequence: A systematic review and meta-analysis.
[object Object], [object Object], [object Object] et al. · Early Hum Dev · 2025
PMID: 39733593Meta-Analysis
The oral and maxillofacial manifestations of Stickler syndrome: A systematic review.
[object Object], [object Object], [object Object] et al. · J Stomatol Oral Maxillofac Surg · 2025
PMID: 39870193Meta-Analysis
Pre-Operative Characteristics Helping to Avoid Gastrostomy Tube After Mandibular Distraction in Neonates With Pierre-Robin Sequence: A Institutional Case-Series and Review of the Literature.
[object Object], [object Object], [object Object] et al. · Ann Otol Rhinol Laryngol · 2024
Non-operative interventions for Pierre-Robin sequence: A systematic review and meta-analysis.
[object Object], [object Object], [object Object] et al. · J Craniomaxillofac Surg · 2024
PMID: 39256141Meta-Analysis
Systematic review and meta-analysis of surgical approaches for improving airway stability in infants with Robin sequence: evaluating complications and outcomes.
[object Object], [object Object], [object Object] et al. · Br J Oral Maxillofac Surg · 2024
PMID: 38845304Meta-Analysis
Therapeutic Management with Airway Clearance in Children with Robin Sequence and Association with Swallowing Outcomes: A Systematic Review and Meta-analysis.
[object Object], [object Object], [object Object] et al. · Dysphagia · 2023
PMID: 36763186Meta-Analysis
Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study.
[object Object], [object Object], [object Object] et al. · Arch Dis Child · 2023
Search all PubMed articles for Robin sequence
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cleft of palate
Very frequent (80-99%)HP:0000175
Decreased projection of mandible
Very frequent (80-99%)HP:0000347
Retraction of the tongue
Very frequent (80-99%)HP:0000162
Feeding difficulties in infancy
Frequent (30-79%)HP:0008872
Hypoxemia
Frequent (30-79%)HP:0012418
Increased amniotic fluid index
Frequent (30-79%)HP:0001561
Respiratory distress, neonatal
Frequent (30-79%)HP:0002643
Undergrowth
Frequent (30-79%)HP:0001508
Upper airway obstruction
Frequent (30-79%)HP:0002781
Blue discoloration of the skin
Occasional (5-29%)HP:0000961
Bronchomalacia
Occasional (5-29%)HP:0002780
Choanal atresia
Occasional (5-29%)HP:0000453
Cor pulmonale
Occasional (5-29%)HP:0001648
Deglutition disorder
Occasional (5-29%)HP:0002015
Floppy windpipe
Occasional (5-29%)HP:0002779
increased pulmonary artery pressure
Occasional (5-29%)HP:0004890
Laryngomalacia
Occasional (5-29%)HP:0001601
Narrowing of windpipe
Occasional (5-29%)HP:0002777
Noisy breathing
Occasional (5-29%)HP:0010307
Sleep apnea
Occasional (5-29%)HP:0010535
Subglottic stenosis
Occasional (5-29%)HP:0001607
Pierre-Robin sequence
HP:0000201
Related Conditions
Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome(child)
Pierre Robin sequence faciodigital anomaly syndrome(child)
Robin sequence with cleft mandible and limb anomalies syndrome(child)
Intellectual disability, brachydactyly, Pierre Robin syndrome(child)
Robin sequence and oligodactyly syndrome(child)
5q23 microdeletion syndrome(child)
Multiple malformation syndrome with facial defects as major feature(parent)
Quick Facts
- SNOMED CT
- 4602007
- UMLS CUI
- C0031900
- Fully Specified Name
- Robin sequence (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.