PREVENTION OF BIRTH OF A SICK BABY IN PATIENTS WITH INFERTILITY AND ROBERTSONIAN TRANSLOCATION IN THE KARYOTYPE


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Acesso é pago ou somente para assinantes

Resumo

The paper describes a clinical observation of a married couple with infertility, heterozygous CYP 21B gene mutation in the wife and Robertsonian translocation in the husband, who have undergone preimplantation and prenatal diagnoses.

Texto integral

Acesso é fechado

Sobre autores

Zh. GLINKINA

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Email: z_glinkina@oparina4.ru
Moscow

K. ALIYEVA

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Moscow

T. BUGAI

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Moscow

N. BELYAEVA

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Moscow

Z. GUBAYEVA

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Moscow

S. SOKUR

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Moscow

E. KALININA

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development of the Russian Federation

Moscow

Bibliografia

  1. Курило Л.Ф., Дубинская В.П., Остроумова Т.В. и др. Анализ патологии сперматогенеза различной этиологии по эякуляту // Пробл. репрод. - 1995. - № 3. - С. 33-38.
  2. Balkan M., Tekes S., Gedik A. Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey // J. Assist. Reprod. Genet. - 2008. - Vol. 25, № 11-12. -Р. 559-565.
  3. Causio F., Fischetto R., Schonauer L.M. et al. Intracytoplasmic sperm injection in infertile patients with structural cytogenetic abnormalities // J. Reprod. Med. - 1999. - Vol. 44, № 10. -P. 859-864.
  4. Goel H., Phadke S.R. Reciprocal balanced translocation: infertility and recurrent spontaneous abortions in a family // Andrologia. - 2011. - Vol. 43, № 1. - P. 75-77.
  5. Keymolen K., Staessen C., Verpoest W. et al. A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosis // Hum. Reprod. - 2009. - Vol. 24, № 9. -Р. 2365-2371.
  6. Loan D., Dumitrii J., Museteanu P. et al. Cytogenetic investigation in 300 couples with recurrent fetal wastage // Rev. Roum. Med. Endocrinol. - 1987. - Vol. 25, № 3. -P. 145-148.
  7. Riccaboni A., Lalatta F., Caliari I. Genetic screening in 2,710 infertile candidate couples for assisted reproductive techniques: results of application of Italian guidelines for the appropriate use of genetic tests // Fertil. and Steril. - 2008. -Vol. 89, № 4. - Р. 800-808.
  8. Yatsenko A.N., Yatsenko S.A., Weedin J.W. Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men // J. Urol. (Baltimore). - 2010. - Vol. 183, № 4. - Р. 1636-1642.

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Bionika Media, 2012

Este site utiliza cookies

Ao continuar usando nosso site, você concorda com o procedimento de cookies que mantêm o site funcionando normalmente.

Informação sobre cookies