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Genetics for the ophthalmologist
Oman Journal of Ophthalmology. 2012; 5 (3): 144-149
em Inglês | IMEMR | ID: emr-155652
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
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Oftalmologia / Linhagem / Retinoblastoma / Defeitos da Visão Cromática / Cromossomos / Atrofia Óptica Hereditária de Leber / Olho / Genes Limite: Humanos Idioma: Inglês Revista: Oman J. Ophthalmol. Ano de publicação: 2012

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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Oftalmologia / Linhagem / Retinoblastoma / Defeitos da Visão Cromática / Cromossomos / Atrofia Óptica Hereditária de Leber / Olho / Genes Limite: Humanos Idioma: Inglês Revista: Oman J. Ophthalmol. Ano de publicação: 2012