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Genetics for the ophthalmologist

Authors :
Karthikeyan A Sadagopan
Jenina Capasso
Alex V Levin
Source :
Oman Journal of Ophthalmology, Vol 5, Iss 3, Pp 144-149 (2012)
Publication Year :
2012
Publisher :
Wolters Kluwer Medknow Publications, 2012.

Abstract

The eye has played a major role in human genomics including gene therapy. It is the fourth most common organ system after integument (skin, hair and nails), nervous system, and musculoskeletal system to be involved in genetic disorders. The eye is involved in single gene disorders and those caused by multifactorial etiology. Retinoblastoma was the first human cancer gene to be cloned. Leber hereditary optic neuropathy was the first mitochondrial disorder described. X-Linked red-green color deficiency was the first X-linked disorder described. The eye, unlike any other body organ, allows directly visualization of genetic phenomena such as skewed X-inactivation in the fundus of a female carrier of ocular albinism. Basic concepts of genetics and their application to clinical ophthalmological practice are important not only in making a precise diagnosis and appropriate referral, but also in management and genetic counseling.

Details

Language :
English
ISSN :
0974620X
Volume :
5
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Oman Journal of Ophthalmology
Publication Type :
Academic Journal
Accession number :
edsdoj.19514062d5694c58b90e1e57ae92147d
Document Type :
article
Full Text :
https://doi.org/10.4103/0974-620X.106092