An 8-year-old child, daughter of Omani parents, presented to the pediatric ophthalmology clinic of Sultan Qaboos University Hospital, Oman, with defective vision, photophobia, and rapid movements of both eyes since birth. The child was otherwise healthy. Both parents were healthy and the marriage was first degree consanguineous. There was a positive family history of similar problems in the patient’s younger brother and paternal aunt. Clinical examination concluded with the diagnosis of oculocutaneous albinism. The patient’s sibling was also examined and diagnosed with the same condition.
An 8-year-old child, daughter of Omani parents, presented to the pediatric ophthalmology clinic of Sultan Qaboos University Hospital, Oman, with defective vision, photophobia, and rapid movements of both eyes since birth. The child was otherwise healthy. Both parents were healthy and the marria...
مادة فرعية
Oman Journal of Ophthalmology