"Facies" 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.
The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or the mongoloid facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed)
| Descriptor ID |
D019066
|
| MeSH Number(s) |
C23.550.291.812 E01.370.600.230
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Facies".
Below are MeSH descriptors whose meaning is more specific than "Facies".
This graph shows the total number of publications written about "Facies" by people in this website by year, and whether "Facies" 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 | 0 | 1 | 1 |
| 2017 | 1 | 3 | 4 |
| 2018 | 0 | 7 | 7 |
To return to the timeline, click here.
Below are the most recent publications written about "Facies" by people in Profiles.
-
Courage Facies. Acad Med. 2021 07 01; 96(7):937-938.
-
New Insights into Kleefstra Syndrome: Report of Two Novel Cases with Previously Unreported Features and Literature Review. Cytogenet Genome Res. 2018; 156(3):127-133.
-
Femoral-facial syndrome: A review of the literature and 14 additional patients including a monozygotic discordant twin pair. Am J Med Genet A. 2018 09; 176(9):1917-1928.
-
Possible Congenital Zika Syndrome in Older Children Due to Earlier Circulation of Zika Virus. Am J Med Genet A. 2018 09; 176(9):1882-1889.
-
A patient with peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and severe hypoganglionosis associated with a novel SOX10 mutation. Am J Med Genet A. 2018 05; 176(5):1195-1199.
-
Integrating Functional Analysis in the Next-Generation Sequencing Diagnostic Pipeline of RASopathies. Sci Rep. 2018 02 05; 8(1):2421.
-
Perthes disease: A new finding in Floating-Harbor syndrome. Am J Med Genet A. 2018 03; 176(3):703-706.
-
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care. Genet Med. 2018 09; 20(9):965-975.
-
A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome. Am J Med Genet A. 2017 10; 173(10):2838-2843.
-
Identification of a novel FOXL2 mutation in a single family with both types of blepharophimosis--ptosis-epicanthus inversus syndrome. Mol Med Rep. 2017 Oct; 16(4):5529-5532.