"Hypertelorism" 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.
Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
| Descriptor ID |
D006972
|
| MeSH Number(s) |
C05.116.099.370.231.480 C05.660.207.231.480 C16.131.621.207.231.480
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Hypertelorism".
Below are MeSH descriptors whose meaning is more specific than "Hypertelorism".
This graph shows the total number of publications written about "Hypertelorism" by people in this website by year, and whether "Hypertelorism" 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 |
|---|
| 1997 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2013 | 0 | 3 | 3 |
| 2014 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Hypertelorism" by people in Profiles.
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Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3. Am J Med Genet A. 2021 11; 185(11):3446-3458.
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Craniofacial phenotypes associated with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3606-3612.
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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. Am J Hum Genet. 2016 Oct 06; 99(4):991-999.
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. Hum Mol Genet. 2014 Jun 01; 23(11):2888-900.
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Frontonasal and fibrous dysplasia in a patient with unilateral cleft lip and palate. J Craniofac Surg. 2013 Jul; 24(4):e422-4.
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Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment. J Craniofac Surg. 2013 Jul; 24(4):1303-6.
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Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndrome. Clin Dysmorphol. 2013 Apr; 22(2):87-90.
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The non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions. Nucleus. 2012 Jul 01; 3(4):330-4.
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Esco2 promotes neuronal differentiation by repressing Notch signaling. Cell Signal. 2011 Nov; 23(11):1876-84.
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Median facial cleft dysmorphism in three siblings: case report and review of the literature. Cleft Palate Craniofac J. 2010 Jan; 47(1):104-6.