KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME
WITH HETEROZYGOUS P.D50N IN THE GJB2 GENE
IN TWO SERBIAN ADULT PATIENTS
Kalezić T.1,*, Vuković I.2, Stojković M.1, Stanojlović S.1, Karanović J.3,
Brajušković G.3, Savić-Pavićević D.3
*Corresponding Author: Tanja Kalezić, School of Medicine, University of Belgrade; Clinic for Eye
Disease, University Clinical Centre of Serbia, Address: Pasterova Street No 2 , Tel. +381638148843,
e-mail address: tanjakalezic@gmail.com
page: 6
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CONCLUSION
Two Serbian KID patients expand our knowledge of
the phenotype variability among patients carrying GJB2
p.D50N mutation.
Controlled studies on local steroid therapy administration
in KID syndrome are needed in order to improve
our knowledge about this form of therapy.
Declaration of Interest: The authors report no conflicts
of interest. The authors alone are responsible for the
content and writing of this article.
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