Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family
Background: Approximately 205 million pregnancies occur each year in the worldwide. On the other hand, Spontaneous abortion has been reported in 15-20% of all diagnosed pregnancies. The most common cause of spontaneous abortion is chromosomal abnormalities of the embryo. Robertsonian translocation c...
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Veröffentlicht in: | Iranian journal of reproductive medicine 2015-01, Vol.12 (8) |
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Sprache: | eng |
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Zusammenfassung: | Background: Approximately 205 million pregnancies occur each year in
the worldwide. On the other hand, Spontaneous abortion has been
reported in 15-20% of all diagnosed pregnancies. The most common cause
of spontaneous abortion is chromosomal abnormalities of the embryo.
Robertsonian translocation carriers specially 21-14 are the most common
balanced rearrangement among the carrier couples with the history of
spontaneous abortion. In order to search for balanced chromosomal
rearrangement and cytogenetic disorders, 10 members of related family
with consanguinity marriage with the history of recurrent miscarriage
were assessed. Case: Cytogenetic evaluation on the basis G-banding
technique at high resolution was performed in 3 couples and their
related family with the history of idiopathic RSA in order to postulate
any balanced chromosomal rearrangement. Conclusion: six members of them
appeared with robertsonian balanced translocation between chromosome
No.21 to No. 14 with the karyotype of 45, XX, t (14, 21) and 45, XY, t
(14, 21), which this results are in agreement with several similar
works which claimed that the risk of spontaneous abortion in couples
with balanced chromosomal rearrangements is higher compared with
general population. Considering to results of present study, it seems
as if the cytogenetic analysis of couples with the history of recurrent
abortions should be suggested compulsory to estimate the probable
presence of any chromosomal rearrangement. This offer wills valuable
information for genetic consulting. |
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ISSN: | 1680-6433 |