Particularity of genetic counseling in case of a family carriers of structural aberration of chromosome 6

Aleksey Nikolayevich Volkov , Rimma Vitalievna Olennikova , Oksana Ivanovna Ritenkova

Journal of obstetrics and women's diseases ›› 2015, Vol. 64 ›› Issue (5) : 106 -109.

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Journal of obstetrics and women's diseases ›› 2015, Vol. 64 ›› Issue (5) : 106 -109. DOI: 10.17816/JOWD645106-109
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Particularity of genetic counseling in case of a family carriers of structural aberration of chromosome 6

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Abstract

We discuss the case of a family carriers of structural chromosomal aberration del(6)(q24) in two generations. For the first time revealed in 2 year old girl, the aberration has become a reason for family medical and genetic examination, including prenatal cytogenetic diagnosis. The results of clinical and genetic testing of the proband were compared with published data.

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partial monosomy 6q / cytogenetic study / genetic counseling

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Aleksey Nikolayevich Volkov, Rimma Vitalievna Olennikova, Oksana Ivanovna Ritenkova. Particularity of genetic counseling in case of a family carriers of structural aberration of chromosome 6. Journal of obstetrics and women's diseases, 2015, 64(5): 106-109 DOI:10.17816/JOWD645106-109

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Volkov A.N., Olennikova R.V., Ritenkova O.I.

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