 Eye Diseases, Hereditary
"Eye Diseases, Hereditary" 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.
Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
| Descriptor ID |
D015785
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| MeSH Number(s) |
C11.270 C16.320.290
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| Concept/Terms |
Eye Diseases, Hereditary- Eye Diseases, Hereditary
- Disease, Hereditary Eye
- Diseases, Hereditary Eye
- Eye Disease, Hereditary
- Hereditary Eye Disease
- Hereditary Eye Diseases
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Below are MeSH descriptors whose meaning is more general than "Eye Diseases, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Eye Diseases, Hereditary".
This graph shows the total number of publications written about "Eye Diseases, Hereditary" by people in this website by year, and whether "Eye Diseases, Hereditary" 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 |
|---|
| 2001 | 1 | 1 | 2 | | 2009 | 0 | 1 | 1 | | 2013 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Eye Diseases, Hereditary" by people in Profiles.
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Khanna S, Rodriguez SH, Blair MA, Wroblewski K, Shapiro MJ, Blair MP. Laser Prophylaxis in Patients with Stickler Syndrome. Ophthalmol Retina. 2022 04; 6(4):263-267.
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Solinski MA, Blair MP, Dietz H, Mittelman D, Shapiro MJ. FEVR findings in patients with Loeys-Dietz syndrome type II. Ophthalmic Genet. 2018 12; 39(6):754-758.
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Lam S, Guimaraes C, Jones JY. Congenital Mydriasis With Aortic and Cerebrovascular Disease. Pediatr Neurol. 2017 09; 74:100-101.
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McAnany JJ, Alexander KR, Kumar NM, Ying H, Anastasakis A, Fishman GA. Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation. Ophthalmic Genet. 2013 Sep; 34(3):167-73.
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Maselli RA, Ng JJ, Anderson JA, Cagney O, Arredondo J, Williams C, Wessel HB, Abdel-Hamid H, Wollmann RL. Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome. J Med Genet. 2009 Mar; 46(3):203-8.
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Reidy JJ. Penetrating keratoplasty in infancy and early childhood. Curr Opin Ophthalmol. 2001 Aug; 12(4):258-61.
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Cormand B, Pihko H, Bayés M, Valanne L, Santavuori P, Talim B, Gershoni-Baruch R, Ahmad A, van Bokhoven H, Brunner HG, Voit T, Topaloglu H, Dobyns WB, Lehesjoki AE. Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease. Neurology. 2001 Apr 24; 56(8):1059-69.
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