ABSTRACT
Jeavons syndrome is a rare generalized childhood epileptic condition characterized by eyelid myoclonia with or without absences. Other features of the syndrome include photosensitivity and electroencephalography [EEC] findings
An eight-year-old male was referred to the pediatric clinic from the ophthalmology clinic with a chief complaint of repetitive abnormal eye movements. The patient did not exhibit any photosensitivity but his EEG was diagnostic for primary generalized epilepsy. Treatment with levetiracetam revealed significant improvement
Subject(s)
Humans , Male , Child , Syndrome , Electroencephalography , SeizuresABSTRACT
Ocular Toxoplasmosis is a non-curable infectious disease caused by Toxoplasma Gondii and is one of the leading causes of severe visual impairment due to the involvement of posterior segment of the eye. Involvement of posterior pole causes severe visual impairment in many patients
We report a case of ocular Toxoplasmosis in a 12-year-old female child. The child was clinically diagnosed as having ocular Toxoplasmosis involving the whole posterior pole of the left eye and few parafoveal lesions in the right eye. Follow-up visit revealed new chorioretinitis lesions in the left eye. The patient was treated with oral Spiramycin 1500 mg/day in two divided doses with prednisolone tablet [Img/kg body weight] for a period of 6 weeks. The chorioretinitis lesions regressed in 3 weeks and follow-up one year after cessation of treatment revealed no recurrence. Spiramycin proved to be effective, safe, economic and easy to administer as twice daily oral dose