"Microphthalmos" 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 or developmental anomaly in which the eyeballs are abnormally small.
Descriptor ID |
D008850
|
MeSH Number(s) |
C11.250.566 C16.131.384.666
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Microphthalmos".
Below are MeSH descriptors whose meaning is more specific than "Microphthalmos".
This graph shows the total number of publications written about "Microphthalmos" by people in this website by year, and whether "Microphthalmos" 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 |
---|
2005 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2012 | 0 | 1 | 1 |
2017 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Microphthalmos" by people in Profiles.
-
Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre- and postnatal diagnostic testing in Germany. Am J Med Genet C Semin Med Genet. 2018 06; 178(2):198-205.
-
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nat Genet. 2017 Feb; 49(2):249-255.
-
A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRL. Klin Padiatr. 2013 Jan; 225(1):29-33.
-
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. Eur J Hum Genet. 2009 Oct; 17(10):1207-15.
-
Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome. Eur J Hum Genet. 2005 May; 13(5):563-9.