COMPREHENSIVE GENETIC EVALUATION
OF BULGARIAN CHILDREN WITH
SYNDROMIC CRANIOSYNOSTOSIS
Delchev T.1, Hadjidekova S.2, Bichev S.3, Veleva Ts.1, Boneva I.4, Avdjieva-Tzavella D.1
*Corresponding Author: Trayan Delchev, MD, PhD, Department of Clinical genetics, University
Children Hospital, Medical University of Sofia; Sofia, Bulgaria, Ivan Geshov blvd. No 11,
tel: +359883482376, e-mail: trayan_delchev@abv.bg
page: 6
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AKNOWLEDMENTS
Declaration of Interest: The authors report no conflicts
of interest. The authors alone are responsible for the
content and writing of this article.
Ethics approval: All procedures performed in this
study involving human participants were in accordance
with the ethical standarts of the institutional research
comitee and with the 1964 Helsinki Decladarion and its
later amendments of comparable ethical standarts. The
study was approved by the Ethics Commitee of Medical
Unversity of Sofia.
Consent to participate and for publication: Informed
consent was obtained from all participants, including their
respective family members (and/or legal guardians) before
clinical selection was performed.
Author‘s contributions: main author, corresponding
author, preliminary clinical selection and diagnostics
- T. Delchev; DNA extraction, array CGH screening, array
analysis - S. Hadjidekova; DNA extraction, MLPA
screening - S. Bichev; imaging studies documentation - Ts.
Veleva; conventional cytogenetic analysis - I. Boneva;
coordinator, main consultant, academic science advisor -
D. Avdjieva-Tzavella
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