Academic Journal

Retinal dystrophy associated with Birt-Hogg-Dubé syndrome

التفاصيل البيبلوغرافية
العنوان: Retinal dystrophy associated with Birt-Hogg-Dubé syndrome
المؤلفون: Ma, Jingyi, Sheri, Narin, Carrell, Nathan, Kalluri, Meena, MacDonald, Ian M
المصدر: RETINAL Cases & Brief Reports ; ISSN 1935-1089
بيانات النشر: Ovid Technologies (Wolters Kluwer Health)
سنة النشر: 2024
الوصف: Purpose: Birt-Hogg-Dubé syndrome (BHDS) is an autosomal dominant cancer syndrome characterized by skin fibrofolliculomas, lung cysts, spontaneous pneumothorax, and multifocal renal carcinomas. Ophthalmologic findings associated with BHDS include flecked chorioretinopathy, choroidal melanoma, iris melanocytosis, and eyelid fibrofolliculomas. We present the case of a retinal dystrophy associated with BHDS. Methods: Observational case report. Results: A 48-year-old woman was referred for poor night vision and peripheral visual field loss. She had a past medical history of Birt-Hogg-Dubé syndrome, manifesting as multiple pulmonary cysts and atelectasis of both lungs. Best corrected visual acuity was 20/25 OU. Posterior segment examination revealed significant vessel attenuation and peripheral retinopathy consistent with a retinal dystrophy. Conclusion: This case associates BHDS with retinal pigment epithelial changes and visual field defects. Patients with BHDS should undergo ophthalmological examination as part of their care.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1097/icb.0000000000001611
DOI: 10.1097/ICB.0000000000001611
الاتاحة: http://dx.doi.org/10.1097/icb.0000000000001611
https://journals.lww.com/10.1097/ICB.0000000000001611
رقم الانضمام: edsbas.A34A6868
قاعدة البيانات: BASE
الوصف
DOI:10.1097/icb.0000000000001611