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...
| Prif Awduron: | , , , |
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| Fformat: | Erthygl |
| Iaith: | Russian |
| Cyhoeddwyd: |
Real Time Ltd
2021-09-01
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| Cyfres: | Российский офтальмологический журнал |
| Pynciau: | |
| Mynediad Ar-lein: | https://roj.igb.ru/jour/article/view/726 |