Ocular manifestations of Fraser syndrome in children. A clinical case

A clinical case of rare genetic disease, Fraser syndrome, in a 1.5-month-old infant is presented. Fraser syndrome is a congenital pathology characterized by diverse clinical symptoms, which involves a combination of acrofacial and urogenital abnormalities and may be accompanied by cryptophtalmos (an...

詳細記述

書誌詳細
主要な著者: T. V. Sudovskaya, L. V. Kogoleva, T. N. Kiseleva, A. N. Bedretdinov
フォーマット: 論文
言語:Russian
出版事項: Real Time Ltd 2021-09-01
シリーズ:Российский офтальмологический журнал
主題:
オンライン・アクセス:https://roj.igb.ru/jour/article/view/726