Congenital Cone-Rod Dystrophy to Progressing Central Vision Loss: A Low Vision Case Report
Kyl Kino I. Dalangin, Sherwin William B. Suarez
Kyl Kino I. Dalangin
Available Online 8 June 2020.
- 10.2991/ahsr.k.200523.053How to use a DOI?
- cone-rod dystrophy, hereditary, extensive ocular examinations
Cone-rod dystrophy is considered to be one of the rare ocular diseases that arises hereditarily. The nature of the disease can easily be mistaken with other ocular condition due to its unusual characteristics. This case report covers extensive ocular examinations and proper management of the condition.
- © 2020, the Authors. Published by Atlantis Press.
- Open Access
- This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).
Cite this article
TY - CONF AU - Kyl Kino I. Dalangin AU - Sherwin William B. Suarez PY - 2020 DA - 2020/06/08 TI - Congenital Cone-Rod Dystrophy to Progressing Central Vision Loss: A Low Vision Case Report BT - The proceedings of the 2nd Bakti Tunas Husada-Health Science International Conference (BTH-HSIC 2019) PB - Atlantis Press SP - 219 EP - 221 SN - 2468-5739 UR - https://doi.org/10.2991/ahsr.k.200523.053 DO - 10.2991/ahsr.k.200523.053 ID - Dalangin2020 ER -