Aniridia: Recent Developments in Scientific and Clinical Research. Questo articolo non è disponibile.
Parekh, Mohit (Editor) / Poli, Barbara (Editor) / Ferrari, Stefano (Editor) / Teofili, Corrado (Editor) / Ponzin, Diego (Editor)
Lingua: inglese
Editore: Springer, 2016
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reprint edition. 192 pages. 9.25x6.10x0.47 inches. In Stock.
Codice articolo __3319363948
- Titolo
- Aniridia: Recent Developments in Scientific and Clinical Research
- Autore
- Parekh, Mohit (Editor) / Poli, Barbara (Editor) / Ferrari, Stefano (Editor) / Teofili, Corrado (Editor) / Ponzin, Diego (Editor)
- Editore
- Springer
- Anno di pubblicazione
- 2016
- Condizione
- Brand New
- Rilegatura
- Paperback
- Lingua
- inglese
- ISBN 10
- 3319363948
- ISBN 13
- 9783319363943
- Peso dell'articolo
- 3,48 chilogrammi
The aim of this book is to highlight the latest findings in Aniridia research. Aniridia, meaning “without iris”, is a rare genetic disorder affecting vision, characterized by the incomplete formation of the iris (the coloured part of the eye that surrounds the black pupil). It may also cause other segments of the eye to be under-developed such as the optic nerve and the macula (the central part of the retina). Aniridia and associated conditions affect individuals differently. So while some affected people are partially sighted or blind, others may have near normal sight. Aniridia is congenital (present at birth) and is caused by a dysfunction of the PAX6 gene, situated on the 11th chromosome that causes the premature cessation of eye development. Aniridia affects between 1:40,000 to 1:100,000 people, and affects males and females equally. People with Aniridia may also experience secondary conditions such as Photophobia, Nystagmus, Glaucoma, Cataracts and Keratopathy.
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Dalla quarta di copertina
? The aim of this book is to highlight the latest findings in Aniridia research. Aniridia, meaning “without iris”, is a rare genetic disorder affecting vision, characterized by the incomplete formation of the iris (the coloured part of the eye that surrounds the black pupil). It may also cause other segments of the eye to be under-developed such as the optic nerve and the macula (the central part of the retina). Aniridia and associated conditions affect individuals differently. So while some affected people are partially sighted or blind, others may have near normal sight. Aniridia is congenital (present at birth) and is caused by a dysfunction of the PAX6 gene, situated on the 11th chromosome that causes the premature cessation of eye development. Aniridia affects between 1:40,000 to 1:100,000 people, and affects males and females equally. People with Aniridia may also experience secondary conditions such as Photophobia, Nystagmus, Glaucoma, Cataracts and Keratopathy.
"Descrizione articolo" può appartenere a un’altra edizione di questo titolo.