 Pierre Robin Syndrome
"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.
An autosomal recessive disorder characterized by brachygnathia and cleft palate, often associated with glossoptosis, backward and upward displacement of the larynx, and angulation of the manubrium sterni. Cleft palate makes sucking and swallowing difficult, permitting easy access of fluids into the larynx. It may appear in several syndromes or as an isolated hypoplasia. (Dorland, 27th ed)
| 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
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| Concept/Terms |
Pierre Robin Syndrome- Pierre Robin Syndrome
- Robin Syndrome, Pierre
- Syndrome, Pierre Robin
- Glossoptosis, Micrognathia, and Cleft Palate
- Pierre-Robin Syndrome
- Syndrome, Pierre-Robin
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
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| 2011 | 1 | 0 | 1 | | 2013 | 1 | 1 | 2 | | 2016 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 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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Prescher H, Froimson JR, Haravu PN, Reid RR. 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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Humphries LS, Reid RR, Ross CF, Taylor AB, Collins JM, Freire AR, Rossi AC, Prado FB. 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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Humphries LS, Yates EK, Mhlaba JM, Collins JM, Baroody FM, Reid RR. Airway Volume Simulation in Virtual Mandibular Distraction: A Cohort Study. Plast Reconstr Surg. 2018 04; 141(4):1003-1009.
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Zellner EG, Reid RR, Steinbacher DM. The Pierre Robin Mandible is Hypoplastic and Morphologically Abnormal. J Craniofac Surg. 2017 Nov; 28(8):1946-1949.
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Zellner EG, Mhlaba JM, Reid RR, Steinbacher DM. Does Mandibular Distraction Vector Influence Airway Volumes and Outcome? J Oral Maxillofac Surg. 2017 Jan; 75(1):167-177.
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Tan HL, Kheirandish-Gozal L, Abel F, Gozal D. Craniofacial syndromes and sleep-related breathing disorders. Sleep Med Rev. 2016 Jun; 27:74-88.
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Johnston JJ, Sapp JC, Curry C, Horton M, Leon E, Cusmano-Ozog K, Dobyns WB, Hudgins L, Zackai E, Biesecker LG. 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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Bhoj E, Halbach S, McDonald-McGinn D, Tan C, Lande R, Waggoner D, Zackai E. 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.
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Gripp KW, Hopkins E, Johnston JJ, Krause C, Dobyns WB, Biesecker LG. Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene. Am J Med Genet A. 2011 Oct; 155A(10):2516-20.
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