File:Oculocutaneous albinism eyes.jpg

Figure 20: OCA1A patient eyes

The image shows the eyes of a patient with OCA1A. The iris is observed to be fully translucent and an ‘almost pink’ colour due to the lack of pigment development.

Reference

Grønskov, K., Ek, J. and Brondum-Nielsen, K. (2007). Oculocutaneous albinism. Orphanet Journal of Rare Diseases, 2(1), p.43.

Mark Hill (talk) 17:12, 30 October 2018 (AEDT) Shown below is the correct referencing format that should have been used here.

Grønskov K, Ek J & Brondum-Nielsen K. (2007). Oculocutaneous albinism. Orphanet J Rare Dis , 2, 43. PMID: 17980020 DOI.

Copyright

© Grønskov et al; licensee BioMed Central Ltd. 2007

Mark Hill (talk) 08:59, 1 November 2018 (AEDT) All required information included. You could have given a little more detail to the description, including spelling out the acronym OCA1A as Oculocutaneous albinism, including a link to the OMIM entry for this disorder OMIM 203100 OCA1A

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