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Richardo Rusli
Falkutas Kedokteran UKRIDA, Jakarta, Indonesia
Health Professions Medicine & Pharmacology Public Health

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Retinitis Pigmentosa Richardo Rusli
Cermin Dunia Kedokteran Vol 47, No 7 (2020): Bedah
Publisher : PT. Kalbe Farma Tbk.

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.55175/cdk.v47i7.597

Abstract

Retinitis pigmentosa merupakan sekelompok penyakit degenerasi retina herediter yang ditandai oleh disfungsi progresif fotoreseptor disertai hilangnya sel secara progresif dan akhirnya menyebabkan atrofi beberapa lapisan retina. Beberapa kasus retinitis pigmentosa merupakan penyakit genetik yang diturunkan secara Mendel. Pada funduskopi, dapat ditemukan perubahan pigmen retina seperti bone spicules. ERG menunjukkan dominasi penurunan amplitudo gelombang-b dalam kondisi skotopik. Farmakoterapi vitamin A, Docosahexaenoic acid (DHA), lutein/zeaxanthin bertujuan untuk mengurangi morbiditas dan mencegah komplikasi.Retinitis pigmentosa is a group of hereditary retinal degeneration characterized by progressive photoreceptor dysfunction and is accompanied by progressive cell loss and eventually causes atrophy in several layers of the retina. Almost all types of retinitis pigmentosa are inherited, caused by errors in genetic information. In funduscopy, changes in retinal pigment can be found in the form of bone spicules. ERG shows a decrease in the b-wave amplitude that dominates in scotopic conditions. Pharmacotherapy such as vitamin A, docosahexaenoic acid (DHA), lutein / zeaxanthin aims to reduce morbidity and prevent complications.
Retinitis Pigmentosa Richardo Rusli
Cermin Dunia Kedokteran Vol. 47 No. 5 (2020): Bedah
Publisher : PT Kalbe Farma Tbk.

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.55175/cdk.v47i5.378

Abstract

Retinitis pigmentosa merupakan sekelompok penyakit degenerasi retina herediter yang ditandai oleh disfungsi progresif fotoreseptor disertai hilangnya sel secara progresif dan akhirnya menyebabkan atrofi beberapa lapisan retina. Beberapa kasus retinitis pigmentosa merupakan penyakit genetik yang diturunkan, dikarenakan kelainan pada informasi genetik. Pada funduskopi, dapat ditemukan perubahan pigmen retina seperti bone spicules. ERG menunjukkan dominasi penurunan amplitudo gelombang-b dalam kondisi skotopik. Farmakoterapi seperti vitamin A, docosahexaenoic acid (DHA), dan lutein/zeaxanthin bertujuan untuk mengurangi morbiditas dan mencegah komplikasi. Retinitis pigmentosa is a group of hereditary retinal degeneration characterized by progressive photoreceptor dysfunction and is accompanied by progressive cell loss and eventually causes atrophy in several layers of the retina. Almost all types of retinitis pigmentosa are inherited, caused by errors in genetic information. In funduscopy, changes in retinal pigment can be found in the form of bone spicules. ERG shows a decrease in the b-wave amplitude that dominates in scotopic conditions. Pharmacotherapy such as vitamin A, docosahexaenoic acid (DHA), and lutein/zeaxanthin, aims to reduce morbidity and prevent complications.
Retinitis Pigmentosa Richardo Rusli
Cermin Dunia Kedokteran Vol 47 No 5 (2020): Bedah
Publisher : PT Kalbe Farma Tbk.

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.55175/cdk.v47i5.378

Abstract

Retinitis pigmentosa merupakan sekelompok penyakit degenerasi retina herediter yang ditandai oleh disfungsi progresif fotoreseptor disertai hilangnya sel secara progresif dan akhirnya menyebabkan atrofi beberapa lapisan retina. Beberapa kasus retinitis pigmentosa merupakan penyakit genetik yang diturunkan, dikarenakan kelainan pada informasi genetik. Pada funduskopi, dapat ditemukan perubahan pigmen retina seperti bone spicules. ERG menunjukkan dominasi penurunan amplitudo gelombang-b dalam kondisi skotopik. Farmakoterapi seperti vitamin A, docosahexaenoic acid (DHA), dan lutein/zeaxanthin bertujuan untuk mengurangi morbiditas dan mencegah komplikasi. Retinitis pigmentosa is a group of hereditary retinal degeneration characterized by progressive photoreceptor dysfunction and is accompanied by progressive cell loss and eventually causes atrophy in several layers of the retina. Almost all types of retinitis pigmentosa are inherited, caused by errors in genetic information. In funduscopy, changes in retinal pigment can be found in the form of bone spicules. ERG shows a decrease in the b-wave amplitude that dominates in scotopic conditions. Pharmacotherapy such as vitamin A, docosahexaenoic acid (DHA), and lutein/zeaxanthin, aims to reduce morbidity and prevent complications.
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