"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 |
|---|
| 2008 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hypertelorism" by people in Profiles.
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Reis LM, Maheshwari M, Capasso J, Atilla H, Dudakova L, Thompson S, Zitano L, Lay-Son G, Lowry RB, Black J, Lee J, Shue A, Kremlikova Pourova R, Vaneckova M, Skalicka P, Jedlickova J, Trkova M, Williams B, Richard G, Bachman K, Seeley AH, Costakos D, Glaser TM, Levin AV, Liskova P, Murray JC, Semina EV. Axenfeld-Rieger syndrome: more than meets the eye. J Med Genet. 2023 04; 60(4):368-379.
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Kantarci S, Ragge NK, Thomas NS, Robinson DO, Noonan KM, Russell MK, Donnai D, Raymond FL, Walsh CA, Donahoe PK, Pober BR. Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy. Am J Med Genet A. 2008 Jul 15; 146A(14):1842-7.