THE INCIDENCE AND TYPE OF CHROMOSOMAL
TRANSLOCATIONS FROM PRENATAL DIAGNOSIS
OF 3800 PATIENTS IN THE REPUBLIC OF MACEDONIA
Vasilevska M1,*, Ivanovska E1, Kubelka Sabit K1, Sukarova-Angelovska E2, Dimeska G3
*Corresponding Author: Marinela Vasilevska, M.Sc., Department of Diagnostic Laboratories, Clinical Hospital
Acibadem-Sistine, Skupi 5A, 1000 Skopje, Republic of Macedonia; Tel.: +389-2-3099-511; Fax: +389-2-
3099-599; vasilevskam@acibademsistina.com.mk
page: 23
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CONCLUSIONS
Most of the prenatal chromosomal translocations
were the result of familial translocations. We detected
three de novo translocations, one balanced X-autosome
translocation, one unbalanced t(18;21)(p11;q11),18pand
one unbalanced der(13;13). The frequency of all translocations was 0.42%. In each case, genetic counseling
was required to establish whether the parents
were heterozygous for the same translocation and to
establish the recurrence risk for future pregnancies.
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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