Authors:
Goura Chattannavar, MBBS, DNB, Flaum Eye Institute, University of Rochester, New York, US; L V Prasad Eye Institute, Hyderabad, India
Alex V Levin, MD, MHSc, Flaum Eye Institute, University of Rochester, New York, US
An optometrist has referred two 8-year-old twin boys, initially seen after they failed a vision screening at school. The children were having difficulty seeing small letters on the blackboard and had reduced night vision (nyctalopia). One of the twins had a history of frequent falls and collisions with objects. Otherwise, growth and development were typical for their age and they were healthy. Family history revealed that their maternal uncle had “retinitis pigmentosa” diagnosed in childhood, and their maternal great–grandfather experienced nyctalopia and vision loss in his early years. There is no parental consanguinity and the families do not have any common ancestry. Examination revealed similar and symmetrical findings in both siblings’ retinas.
Authors:
Goura Chattannavar, MBBS, DNB, Flaum Eye Institute, University of Rochester, New York, US; L V Prasad Eye Institute, Hyderabad, India
Alex V Levin, MD, MHSc, Flaum Eye Institute, University of Rochester, New York, US
thanks
Ok
Very nice. Makes us think and remeber basic concepts of genetics.
GOOD!
Thanks
Very good one
Nice
Wow
It is very interesting case. Thank you very much.
Awesome!! Keep sharing.
Thank you Dr. Chattannavar and Dr. Levin
I can do it
Amazing case description, thank you so much for sharing.
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Excellent
Nice case
Nice
Very helpfull, thank you very much
This work is very interesting.
Thanks
Really appreciate it
Very interesting case
Ok