Ectopia Lentis

"Ectopia Lentis" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Congenital displacement of the lens resulting from defective zonule formation.

Descriptor ID

D004479

MeSH Number(s)

C11.250.300

C11.510.598.373

C16.131.384.405

Concept/Terms

Ectopia Lentis

Below are MeSH descriptors whose meaning is more general than "Ectopia Lentis".

Diseases [C]
Eye Diseases [C11]
Eye Abnormalities [C11.250]
Ectopia Lentis [C11.250.300]
Lens Diseases [C11.510]
Lens Subluxation [C11.510.598]
Ectopia Lentis [C11.510.598.373]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Eye Abnormalities [C16.131.384]
Ectopia Lentis [C16.131.384.405]

Below are MeSH descriptors whose meaning is related to "Ectopia Lentis".

Below are MeSH descriptors whose meaning is more specific than "Ectopia Lentis".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Ectopia Lentis" by people in Harvard Catalyst Profiles by year, and whether "Ectopia Lentis" was a major or minor topic of these publication.

Bar chart showing 16 publications over 12 distinct years, with a maximum of 2 publications in 2009 and 2014 and 2015 and 2016

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2001	1	0	1
2006	1	0	1
2009	1	1	2
2010	0	1	1
2011	1	0	1
2012	0	1	1
2013	1	0	1
2014	1	1	2
2015	2	0	2
2016	2	0	2
2020	1	0	1
2022	1	0	1

Below are the most recent publications written about "Ectopia Lentis" by people in Profiles.

Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort. Genet Med. 2022 05; 24(5):1045-1053.

View in: PubMed
Latent-transforming growth factor beta-binding protein-2 (LTBP-2) is required for longevity but not for development of zonular fibers. Matrix Biol. 2021 01; 95:15-31.

View in: PubMed
Capsular bag stabilization during lens extraction and intraocular lens implantation in cases of Marfan syndrome with ectopia lentis using ultra-high-viscosity ophthalmic viscosurgical devices. J Cataract Refract Surg. 2016 10; 42(10):1397-1401.

View in: PubMed
Persistent Blurry Vision After a Routine Eye Examination. JAMA Ophthalmol. 2016 09 01; 134(9):1065-6.

View in: PubMed
Early onset ectopia lentis due to a FBN1 mutation with non-penetrance. Am J Med Genet A. 2015 Jun; 167(6):1365-8.

View in: PubMed
Trauma-Induced Bilateral Ectopia Lentis Diagnosed with Point-of-Care Ultrasound. J Emerg Med. 2015 Jun; 48(6):e135-7.

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Recessive mutations in LEPREL1 underlie a recognizable lens subluxation phenotype. Ophthalmic Genet. 2015 Mar; 36(1):58-63.

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Latent TGF-ß binding protein-2 is essential for the development of ciliary zonule microfibrils. Hum Mol Genet. 2014 Nov 01; 23(21):5672-82.

View in: PubMed
Mutations in ASPH cause facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs, or Traboulsi syndrome. Am J Hum Genet. 2014 May 01; 94(5):755-9.

View in: PubMed
Genetics of ectopia lentis. Semin Ophthalmol. 2013 Sep-Nov; 28(5-6):313-20.

View in: PubMed

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