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...
| Hlavní autoři: | , , , |
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| Médium: | Článek |
| Jazyk: | Russian |
| Vydáno: |
Real Time Ltd
2021-09-01
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| Edice: | Российский офтальмологический журнал |
| Témata: | |
| On-line přístup: | https://roj.igb.ru/jour/article/view/726 |