الملخص
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.
بيانات النشر
- المعرّف الرقمي
- 10.18295/2075-0528.1168
- المجلة
- مجلة جامعة السلطان قابوس الطبية, 10(1), 111-113
- الناشر
- جامعة السلطان قابوس
- وصول مفتوح
- وصول مفتوح ذهبي
- الترخيص
- CC BY-ND 4.0
اقتبس هذه المقالة
APA 7
Keshav, B. R., Mohammed, M. J., & Nasir (2025). Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports. Sultan Qaboos University Medical Journal, 10(1), 111-113. https://doi.org/10.18295/2075-0528.1168
MLA 9
Keshav, B R., et al. "Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports." Sultan Qaboos University Medical Journal, vol. 10, no. 1, 2025, pp. 111-113. https://doi.org/10.18295/2075-0528.1168.
شيكاغو (المؤلف–التاريخ)
Keshav, B R., Mahmood J. Mohammed, and Nasir. 2025. "Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports." Sultan Qaboos University Medical Journal 10 (1): 111-113. https://doi.org/10.18295/2075-0528.1168.
هارفارد
Keshav, B. R., Mohammed, M. J. and Nasir (2025) 'Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports', Sultan Qaboos University Medical Journal, 10(1), pp. 111-113. doi:10.18295/2075-0528.1168.
فانكوفر
Keshav BR, Mohammed MJ, Nasir. Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports. Sultan Qaboos University Medical Journal. 2025;10(1):111-113. doi:10.18295/2075-0528.1168
IEEE
B. R. Keshav, M. J. Mohammed, and Nasir, "Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports," Sultan Qaboos University Medical Journal, vol. 10, no. 1, pp. 111-113, 2025, doi: 10.18295/2075-0528.1168.