File:Anophthalmia.jpg
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Anophthalmia
Clinical appearance of anophthalmia.
- Anophthalmia - clinical description for the absence of an eye. Gene mutation of SOX2, a developmental transcription factor, has been associated with this condition.
Reference
<pubmed>18039390</pubmed>| Orphanet Journal of Rare Diseases
Copyright
© 2007 Verma and FitzPatrick; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Original file name: 1750-1172-2-47-1.jpg
Cite this page: Hill, M.A. (2024, April 19) Embryology Anophthalmia.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Anophthalmia.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
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| current | 07:42, 7 April 2016 | | 600 × 504 (46 KB) | Z8600021 (talk | contribs) | ==Anophthalmia == Clinical appearance of anophthalmia. * Anophthalmia - clinical description for the absence of an eye. Gene mutation of SOX2, a developmental transcription factor, has been associated with this condition. :'''Links:''' [[Sensory -... |
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