"Pierre Robin Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Congenital malformation characterized by MICROGNATHIA or RETROGNATHIA; GLOSSOPTOSIS and CLEFT PALATE. The mandibular abnormalities often result in difficulties in sucking and swallowing. The syndrome may be isolated or associated with other syndromes (e.g., ANDERSEN SYNDROME; CAMPOMELIC DYSPLASIA). Developmental mis-expression of SOX9 TRANSCRIPTION FACTOR gene on chromosome 17q and its surrounding region is associated with the syndrome.
| Descriptor ID |
D010855
|
| MeSH Number(s) |
C05.500.460.606 C05.660.207.540.460.606 C07.320.440.606 C07.650.500.460.606 C16.131.621.207.540.460.606 C16.131.850.500.460.606
|
| Concept/Terms |
Pierre Robin Syndrome- Pierre Robin Syndrome
- Robin Syndrome, Pierre
- Syndrome, Pierre Robin
- Robin Sequence
- Sequence, Robin
- Pierre Robin's Sequence
- Pierre Robins Sequence
- Sequence, Pierre Robin's
- Pierre-Robin Syndrome
- Syndrome, Pierre-Robin
- Glossoptosis, Micrognathia, and Cleft Palate
- Pierre Robin Sequence
- Sequence, Pierre Robin
|
Below are MeSH descriptors whose meaning is more general than "Pierre Robin Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Pierre Robin Syndrome".
This graph shows the total number of publications written about "Pierre Robin Syndrome" by people in this website by year, and whether "Pierre Robin Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 2 | 2 |
| 2011 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2016 | 2 | 0 | 2 |
| 2017 | 2 | 0 | 2 |
| 2019 | 0 | 2 | 2 |
| 2020 | 6 | 0 | 6 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Pierre Robin Syndrome" by people in Profiles.
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Airway and Feeding Outcomes in Pierre Robin Sequence: A Comparison of Three Management Strategies. Cleft Palate Craniofac J. 2023 06; 60(6):689-694.
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Mandibular and Maxillary Cysts in a Pediatric Patient with Pierre Robin Sequence and Ullrich Congenital Muscular Dystrophy. Anesthesiology. 2020 10 01; 133(4):919-920.
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Mandibular Distraction in Robin Sequence With Multi-Level Airway Disease: Always Contraindicated? J Craniofac Surg. 2020 Oct; 31(7):1883-1887.
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Short-term condylar and glenoid fossa changes in infants with Pierre Robin sequence undergoing mandibular distraction osteogenesis. Int J Oral Maxillofac Surg. 2021 Feb; 50(2):171-178.
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Quantification of Mandibular Morphology in Pierre Robin Sequence to Optimize Mandibular Distraction Osteogenesis. Cleft Palate Craniofac J. 2020 08; 57(8):1032-1040.
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An Intraoperative Salvage After Transection of the Greater Palatine Artery During Cleft Palate Repair: A Case for Buccal Fat and Buccal Myomucosal Flaps. J Craniofac Surg. 2020 Mar/Apr; 31(2):e133-e135.
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Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism. Bone. 2020 04; 133:115219.
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Congenital talipes equinovarus (clubfoot). Am J Obstet Gynecol. 2019 12; 221(6):B10-B12.
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Cervical Stenosis in Non-Syndromic Pierre Robin Sequence. J Craniofac Surg. 2019 Sep; 30(6):1866-1868.
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Difficult airway intubation simulation using Bonfils fiberscope and rigid fiberscope for surgical training. Int J Pediatr Otorhinolaryngol. 2018 Feb; 105:171-175.