 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.
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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Pierre Robin Syndrome" by people in Profiles.
-
McGhee H, Gehle D, Shope C, Wen CC, Marston AP, Discolo C, Pecha PP. Feeding Performance and Outcomes in Infants With Robin Sequence Undergoing Mandibular Distraction Osteogenesis. Cleft Palate Craniofac J. 2024 02; 61(2):295-301.
-
Marston AP, Patel T, Pecha PP, Nguyen SA, Discolo CM. Impact of Hospital Characteristics on Mandibular Distraction Osteogenesis Outcomes Among Patients With Pierre Robin Sequence Utilizing a National Inpatient Database. Cleft Palate Craniofac J. 2022 05; 59(5):622-628.
-
Breik O, Umapathysivam K, Tivey D, Anderson P. Feeding and reflux in children after mandibular distraction osteogenesis for micrognathia: A systematic review. Int J Pediatr Otorhinolaryngol. 2016 Jun; 85:128-35.
-
Kaufman MG, Cassady CI, Hyman CH, Lee W, Watcha MF, Hippard HK, Olutoye OA, Khechoyan DY, Monson LA, Buchanan EP. Prenatal Identification of Pierre Robin Sequence: A Review of the Literature and Look towards the Future. Fetal Diagn Ther. 2016; 39(2):81-9.
-
Pilu G, Romero R, Reece EA, Jeanty P, Hobbins JC. The prenatal diagnosis of Robin anomalad. Am J Obstet Gynecol. 1986 Mar; 154(3):630-2.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|