NOVEL GENOTYPE IN TWO SIBLINGS WITH 5-α-
REDUCTASE 2 DEFICIENCY: DIFFERENT CLINICAL
COURSE DUE TO THE TIME OF DIAGNOSIS
Kocova M1,*, Plaseska-Karanfilska D2, Noveski P2, Kuzmanovska M2
*Corresponding Author: Professor Dr. Mirjana Kocova, University Pediatric Clinic, Department of
Endocrinology & Genetics, M. Tereza 17, Skopje 1000, Republic of North Macedonia. Tel: +389-70-
242-694. Fax: +389-317-6167. E-mail: mirjanakocova@yahoo.com
page: 69
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ACKNOWLEDGMENTS
We acknowledge the collaboration of the patients
from the Department of Surgery Pediatric Surgery and
University Clinic for Gynecology and Obstetrics (Medical
Faculty, Skopje, RN Macedonia), and editing help of
DrMrSci. Elena Kochova (independent consultant).
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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