Two siblings with late-onset cone–rod dystrophy and no visible macular degeneration

Hiroyuki Sakuramoto1 Department of Ophthalmology, Kinki University Faculty of Medicine, Osaka-Sayama City, Osaka, Japan

Kazuki Kuniyoshi1 Department of Ophthalmology, Kinki University Faculty of Medicine, Osaka-Sayama City, Osaka, JapanCorrespondence[email protected]

Kazushige Tsunoda2 National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan

Masakazu Akahori2 National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan

Takeshi Iwata2 National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan

Yoshikazu Shimomura1 Department of Ophthalmology, Kinki University Faculty of Medicine, Osaka-Sayama City, Osaka, Japan

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Xin Jin, Lanlan Chen, Dajiang Wang, Yixin Zhang, Zehua Chen & Houbin Huang. (2018) Novel compound heterozygous mutation in the POC1B gene underlie peripheral cone dystrophy in a Chinese family. Ophthalmic Genetics 39:3, pages 300-306.
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Wajiha Jurdi Kheir, Minzhong Yu, Alfonso Senatore, Alessandro Racioppi, Roberto Gattegna, Donnell Creel & Alessandro Iannaccone. 2019. Handbook of Clinical Electrophysiology of Vision. Handbook of Clinical Electrophysiology of Vision 77 109 .

Takeshi Iwata. 2017. Advances in Vision Research, Volume I. Advances in Vision Research, Volume I 9 19 .

Ewa Langwińska-Wośko, Kamil Szulborski, Anna Zaleska-Żmijewska & Jerzy Szaflik. (2015) Electrophysiological testing as a method of cone–rod and cone dystrophy diagnoses and prediction of disease progression. Documenta Ophthalmologica 130:2, pages 103-109.
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Two siblings with late-onset cone–rod dystrophy and no visible macular degeneration

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Two siblings with late-onset cone–rod dystrophy and no visible macular degeneration

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