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Abstract

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.


Keywords

Albinism Oculocutaneous Axenfeld anomaly Hereditary Consanguinity Association.

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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