"Goldenhar 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.
Mandibulofacial dysostosis with congenital eyelid dermoids.
Descriptor ID |
D006053
|
MeSH Number(s) |
C05.116.099.370.231.576.410 C05.660.207.231.576.410 C16.131.621.207.231.576.410
|
Concept/Terms |
Goldenhar Syndrome- Goldenhar Syndrome
- Goldenhar Disease
- Moeschler Clarren Syndrome
- Oculoauriculovertebral Dysplasia
- Dysplasia, Oculoauriculovertebral
- Dysplasias, Oculoauriculovertebral
- Oculoauriculovertebral Dysplasias
- Oculoauriculovertebral Spectrum
- Oculoauriculovertebral Spectrums
- Oculoauriculovertebral Syndrome
- Craniofacial Microsomia
- Craniofacial Microsomias
- Microsomia, Craniofacial
- Microsomias, Craniofacial
- Facioauriculovertebral Dysplasia
- Dysplasia, Facioauriculovertebral
- Dysplasias, Facioauriculovertebral
- Facioauriculovertebral Dysplasias
- Goldenhar-Gorlin Syndrome
- Goldenhar Gorlin Syndrome
- Goldenhar-Gorlin Syndromes
- Lateral Facial Dysplasia
- Dysplasia, Lateral Facial
- Dysplasias, Lateral Facial
- Facial Dysplasia, Lateral
- Facial Dysplasias, Lateral
- Lateral Facial Dysplasias
- Oral-Mandibular-Auricular Syndrome
- Oral Mandibular Auricular Syndrome
- Oral-Mandibular-Auricular Syndromes
- Otomandibular Dysostosis
- Dysostosis, Otomandibular
- First and Second Pharyngeal Arch Syndromes
- First and Second Branchial Arch Syndrome
- Facioauriculovertebral Sequence
- Facioauriculovertebral Sequences
Goldenhar Syndrome with Ipsilateral Radial Defect- Goldenhar Syndrome with Ipsilateral Radial Defect
- Microsomia Hemifacial Radial Defects
- Oculoauriculovertebral Spectrum with Radial Defect
- Hemifacial Microsomia with Radial Defects
- OAVS with Radial Defect
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Below are MeSH descriptors whose meaning is more general than "Goldenhar Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Goldenhar Syndrome".
This graph shows the total number of publications written about "Goldenhar Syndrome" by people in this website by year, and whether "Goldenhar 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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2008 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2015 | 0 | 1 | 1 |
2019 | 1 | 1 | 2 |
2020 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Goldenhar Syndrome" by people in Profiles.
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FOXI3 pathogenic variants cause one form of craniofacial microsomia. Nat Commun. 2023 04 11; 14(1):2026.
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Counterclockwise Craniofacial Distraction Osteogenesis. Clin Plast Surg. 2021 Jul; 48(3):445-454.
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Airway Obstruction Management With Mandibular Distraction and Matthews Device in Pruzansky III Craniofacial Microsomia. J Craniofac Surg. 2020 May/Jun; 31(3):e277-e280.
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Goldenhar syndrome associated with genital tract abnormality. BMJ Case Rep. 2019 Aug 28; 12(8).
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Cranial Anchored Mandible Distraction Osteogenesis. J Craniofac Surg. 2019 Mar/Apr; 30(2):e183-e186.
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A Geometric Classification of Jaw Deformities. J Oral Maxillofac Surg. 2015 Dec; 73(12 Suppl):S26-31.
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Ectopic external auditory canal and ossicular formation in the oculo-auriculo-vertebral spectrum. Pediatr Radiol. 2015 Jul; 45(7):1099-102.
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Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement. Am J Med Genet A. 2008 Oct 01; 146A(19):2480-9.
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Multiple accessory tragi as a clue to the diagnosis of the oculo-auriculo-vertebral (Goldenhar) syndrome. J Am Acad Dermatol. 2004 Feb; 50(2 Suppl):S11-3.