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Updated: Mar 24, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a
Amina Kurtovic-Kozaric1, Lejla Mehinovic, Meliha Stomornjak-Vukadin
1Department of Pathology, Clinical Center of the University of Sarajevo. amina.kurtovic@gmail.com.
Abstract:
Microdeletion syndromes are caused by chromosomal deletions of less than 5 megabases which can be detected by fluorescence in situ hybridization (FISH). We evaluated the most commonly detected microdeletions for the period from June 01, 2008 to June 01, 2015 in the Federation of Bosnia and Herzegovina, including DiGeorge, Prader-Willi/Angelman, Wolf-Hirschhorn, and Williams syndromes. We report 4 patients with DiGeorge syndromes, 4 patients with Prader-Willi/Angelman, 4 patients with Wolf-Hirschhorn syndrome, and 3 patients with Williams syndrome in the analyzed 7 year period. Based on the positive FISH results for each syndrome, the incidence was calculated for the Federation of Bosnia and Herzegovina. These are the first reported frequencies of the microdeletion syndromes in the Federation of Bosnia and Herzegovina.

