Craniofacial Abnormalities
"Craniofacial Abnormalities" 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 structural deformities, malformations, or other abnormalities of the cranium and facial bones.
| Descriptor ID |
D019465
|
| MeSH Number(s) |
C05.660.207 C16.131.621.207
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Craniofacial Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Craniofacial Abnormalities".
This graph shows the total number of publications written about "Craniofacial Abnormalities" by people in this website by year, and whether "Craniofacial Abnormalities" 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 |
|---|
| 2004 | 0 | 1 | 1 |
| 2017 | 5 | 0 | 5 |
| 2018 | 4 | 0 | 4 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Craniofacial Abnormalities" by people in Profiles.
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Mask on, Mask off: The Role of Comprehensive Craniofacial Care in Addressing Patient Safety and COVID-19 Mandates during School Reopening. Plast Reconstr Surg. 2021 08 01; 148(2):351e-352e.
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Just Breathe: Tips and Highlights for Managing Pediatric Respiratory Distress and Failure. Emerg Med Clin North Am. 2021 Aug; 39(3):493-508.
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The society for craniofacial genetics and developmental biology 43rd annual meeting. Am J Med Genet A. 2021 06; 185(6):1932-1939.
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A Guide to Developing Safety Protocols for International Craniofacial Outreach Programs During the COVID-19 Era. J Craniofac Surg. 2021 Jan-Feb 01; 32(1):e108-e110.
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A Tiered System to Guide Prioritization of Pediatric Cleft and Craniofacial Cases in COVID-19. Plast Reconstr Surg. 2020 09; 146(3):392e-394e.
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Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes. Medicina (Kaunas). 2019 Mar 25; 55(3).
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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.
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Orthopedic-orthodontic treatment of the patient with Turner's syndrome: Review of the literature and case report. Spec Care Dentist. 2018 Jul; 38(4):239-248.
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[A de novo GJA1 mutation identified by whole-exome sequencing in a patient with oculodentodigital dysplasia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10; 35(2):268-271.
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Perthes disease: A new finding in Floating-Harbor syndrome. Am J Med Genet A. 2018 03; 176(3):703-706.