Bilateral retinitis pigmentosa with unilateral choroidal nevus: A hitherto unreported association
نویسندگان
چکیده
منابع مشابه
Unilateral retinitis pigmentosa.
OBJECTIVE To report a rare case of unilateral retinitis pigmentosa and to present the clinical features, and findings of multifocal ERG and visual field of this case. CASE A 70-year-old-female diagnosed as Retinitis Pigmentosa in right eye 7 years back, presented with further gradual painless diminution of vision in the very eye and without any similar symptoms in left eye. On examination, th...
متن کاملUnilateral retinitis pigmentosa sine pigmento.
A patient presented with unilateral findings of night blindness shown by impaired rod function and dark adaptation, constricted visual fields with good central acuity, a barely recordable electro-retinographic b-wave, and a unilaterally impaired electro-oculogram. There were none of the pigmentary changes usually associated with retinitis pigmentosa. The unaffected right eye was normal in all r...
متن کاملBilateral disc edema and unilateral macular hole in a patient with retinitis pigmentosa.
PURPOSE A unique case of retinitis pigmentosa (RP) associated with bilateral disc edema and unilateral macular hole is presented. METHODS A 49-year-old woman, a known RP patient, was found to have bilateral disc edema and a macular hole in the left eye during routine clinical examination. Fluorescein angiography revealed hyperfluorescent leakage of the optic nerve head significantly OD and mi...
متن کامل[Unilateral retinitis pigmentosa or pseudoretinitis pigmentosa? Case report].
Unilateral retinitis pigmentosa is a rare disease characterized by loss of photoreceptors and retinal pigment deposition without affecting the contralateral eye. Although described more than one hundred years its existence is still questioned. This article reports a case of a patient with abnormalities suggestive of unilateral retinitis pigmentosa. The clinical and complementary examinations ar...
متن کاملBilateral congenital nevus of Ota in association with Mongolian spot
A 24-year-old woman presented with asymptomatic hyperpigmented bilateral patches on her temples, eyelids and forehead since birth. Furthermore, the patient had a congenital grey patch, compatible with Mongolian spot, on her buttock. She had no vascular or other cutaneous lesion. Histopathologic examination revealed bipolar dendritic melanocytes dispersed in a ribbon-like pattern between the col...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Saudi Journal of Ophthalmology
سال: 2016
ISSN: 1319-4534
DOI: 10.1016/j.sjopt.2016.01.004