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Foraldy, Thendy
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Health Professions Medicine & Pharmacology Public Health

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Retinitis Pigmentosa pada Laki-laki 27 Tahun Faustine, Giovani; Foraldy, Thendy
Cermin Dunia Kedokteran Vol 47, No 7 (2020): Bedah
Publisher : PT. Kalbe Farma Tbk.

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (500.092 KB) | DOI: 10.55175/cdk.v47i7.600

Abstract

Retinitis pigmentosa merupakan penyakit yang dapat diturunkan secara autosomal-dominant, autosomal-recessive ataupun X-linked. Diperlukan skrining dan edukasi agar penyakit ini dapat dihadapi dengan baik. Kasus. Laki-laki usia 27 tahun dengan gejala nyctalopia, gangguan lapangan pandang, dan gambaran bone spicule pada funduskopi. Didapatkan riwayat dua orang di keluarganya memiliki keluhan sama.Retinitis pigmentosa is an autosomal-dominant, autosomal-recessive or X-linked hereditary disease. Screening and a thorough education is needed. Case: A 27-year old male with symptoms of nyctalopia, visual field decrease, and bone spicule in funduscopy. Two other member of his family also have similar symptoms.
Co-Authors Faustine, Giovani