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.


Links: Anophthalmia and microphthalmia | Anophthalmia | Microphthalmia | Sensory - Vision Abnormalities

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 Image panel cropped, relabelled, and resized from original figure.


Cite this page: Hill, M.A. (2020, September 22) Embryology Anophthalmia.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Anophthalmia.jpg

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© Dr Mark Hill 2020, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G

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current07:42, 7 April 2016Thumbnail for version as of 07:42, 7 April 2016600 × 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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