"Coloboma" 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 anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation.
| Descriptor ID |
D003103
|
| MeSH Number(s) |
C11.250.110 C16.131.384.282
|
| Concept/Terms |
Coloboma- Coloboma
- Colobomas
- Coloboma, Uveoretinal
- Coloboma Of Iris, Choroid, And Retina
- Uveoretinal Coloboma
- Coloboma, Ocular
- Ocular Coloboma
|
Below are MeSH descriptors whose meaning is more general than "Coloboma".
Below are MeSH descriptors whose meaning is more specific than "Coloboma".
This graph shows the total number of publications written about "Coloboma" by people in this website by year, and whether "Coloboma" 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 |
|---|
| 1996 | 0 | 1 | 1 |
| 1997 | 0 | 1 | 1 |
| 1998 | 1 | 0 | 1 |
| 2000 | 0 | 2 | 2 |
| 2001 | 0 | 1 | 1 |
| 2003 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
| 2022 | 2 | 0 | 2 |
| 2024 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Coloboma" by people in Profiles.
-
Chattannavar G, Ger M, Balasubramanian J, Mandal S, Jalali S, Takkar B, Pisuchpen P, de Guimaraes TAC, Capasso JE, Kumar Padhy S, Levin AV. Bardet-Biedl syndrome with chorioretinal coloboma: a case series and review of literature. Ophthalmic Genet. 2024 12; 45(6):616-622.
-
Reis LM, Chassaing N, Bardakjian T, Thompson S, Schneider A, Semina EV. ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes. Eur J Hum Genet. 2023 03; 31(3):363-367.
-
Abdi F, Abdolalizadeh P, Sardarinia M, Gordiz A, Zarastvand F, Hemmati S, Mahmoudzadeh R. The Vascular Pattern In Vicinity Of Chorioretinal Coloboma: An Optical Coherence Tomography Angiography Study. Ophthalmic Genet. 2022 08; 43(4):481-487.
-
Fitzgerald KK, Powell-Hamilton N, Shillingford AJ, Robinson B, Gripp KW. Inherited intragenic PBX1 deletion: Expanding the phenotype. Am J Med Genet A. 2021 01; 185(1):234-237.
-
Wibbelsman TD, Xu D, Garg SJ. Papillorenal Syndrome With Macular Retinoschisis and Subretinal Fluid. JAMA Ophthalmol. 2020 08 01; 138(8):e194774.
-
Pefkianaki M, Schneider A, Capasso JE, Wasserman BN, Bardakjian T, Levin AV. Ocular manifestations of PACS1 mutation. J AAPOS. 2018 08; 22(4):323-325.
-
Bowe T, Rahmani S, Yonekawa Y. Endoscopic Vitrectomy for Microcornea, Posterior Megalolenticonus, Persistent Fetal Vasculature, Coloboma Syndrome. Ophthalmology. 2017 12; 124(12):1742.
-
Rahimy E, Rahimy E. Bilateral Optic Nerve Coloboma and Macular Schisis in Papillorenal Syndrome. Ophthalmology. 2016 05; 123(5):990.
-
Pellegrini M, Shields CL, Arepalli S, Shields JA. Posterior tunica vasculosa lentis and "brittle star" of persistent fetal vasculature. J Pediatr Ophthalmol Strabismus. 2014 Nov 19; 51 Online:e69-71.
-
Arevalo JF, Lasave AF, Arevalo FA, Shields JA. Rhegmatogenous retinal detachment and bilateral optic disc coloboma in organoid nevus syndrome. JAMA Ophthalmol. 2013 Jan; 131(1):111-3.