Main Article Content
Oculocutaneous albinism and anterior mesodermal dysgenesis are well-known heritable conditions, but their occurrence in association has only been rarely reported. We present cases of three siblings of a family with identical presentation suggesting that this association may be more than just a coincidence. This association is worth noting, as this could be one of the causes of ocular morbidity and poor vision in oculocutaneous albinism.
Albinism Oculocutaneous Axenfeld anomaly Hereditary Consanguinity Association.
How to Cite
Keshav, B. R., Mohammed, M. J., & Mahmood, N. (2010). Oculocutaneous Albinism associated with Axenfeld’s Anomaly : Three case reports. Sultan Qaboos University Medical Journal [SQUMJ], 10(1), 111–113. Retrieved from https://journals.squ.edu.om/index.php/squmj/article/view/1460