Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients

Kategoria artykułu: Case report

Data publikacji: 01 mar 2023

Zakres stron: 79 - 84

DOI: https://doi.org/10.2478/bjmg-2022-0014

Słowa kluczowe

gene, keratitis-ichthyosis-deafness syndrome, KID, p.D50N, steroid therapy

© 2022 Kalezić T., Vuković I., Stojković M., Stanojlović S., Karanović J., Brajušković G., Savić-Pavićević D., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.