"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
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| 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 |
|---|
| 2011 | 1 | 0 | 1 |
| 2013 | 1 | 1 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 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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Precise modulation of transcription factor levels identifies features underlying dosage sensitivity. Nat Genet. 2023 05; 55(5):841-851.
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Impact of Cleft Palate on Tongue-Based Upper Airway Obstruction in Pierre Robin Sequence: Implications for Mandibular Distraction Osteogenesis and Timing of Cleft Palate Repair. J Craniofac Surg. 2022 Mar-Apr 01; 33(2):459-462.
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Biomechanical and morphological analysis of Pierre Robin sequence mandible: Finite element and morphometric study. Anat Rec (Hoboken). 2021 07; 304(7):1375-1388.
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Airway Morphological Changes in Pierre Robin Sequence: A Retrospective Study. Cleft Palate Craniofac J. 2020 07; 57(7):828-839.
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Airway Volume Simulation in Virtual Mandibular Distraction: A Cohort Study. Plast Reconstr Surg. 2018 04; 141(4):1003-1009.
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The Pierre Robin Mandible is Hypoplastic and Morphologically Abnormal. J Craniofac Surg. 2017 Nov; 28(8):1946-1949.
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Does Mandibular Distraction Vector Influence Airway Volumes and Outcome? J Oral Maxillofac Surg. 2017 Jan; 75(1):167-177.
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Craniofacial syndromes and sleep-related breathing disorders. Sleep Med Rev. 2016 Jun; 27:74-88.
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Expansion of the TARP syndrome phenotype associated with de novo mutations and mosaicism. Am J Med Genet A. 2014 Jan; 164A(1):120-8.
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Expanding the spectrum of microdeletion 4q21 syndrome: a partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and Pierre Robin sequence. Am J Med Genet A. 2013 Sep; 161A(9):2327-33.