scholarly journals Successful pregnancy in a patient with Swyer syndrome, or pure 46,XY gonadal dysgenesis

2019 ◽  
Vol 25 (1) ◽  
pp. 9
Author(s):  
A Chrysostomou ◽  
M Tsuari
2019 ◽  
Vol 6 (4) ◽  
pp. 225-228
Author(s):  
Elena V. Timokhina ◽  
N. V Afanas’yeva ◽  
Yu. A Samoylova ◽  
T. M Silayeva ◽  
V. S Belousova ◽  
...  

Swyer syndrome (46,XY complete gonadal dysgenesis) is a rare chromosomal pathology. This pathology occurs with a frequency of 1 in 80,000. In genetic analysis, mutations are most often found in the following genes: the SRY gene, the NR5A1 gene, the SOX9 gene, the MAP3K1 gene. Patients with this disease develop phenotypically as women, but due to the absence of gonads and eggs, independent pregnancy is impossible. This article describes a clinical case of a successful onset, course of pregnancy and delivery in a woman with Swyer syndrome using assisted reproductive technology.


2020 ◽  
Vol 11 (3) ◽  
pp. 65-68
Author(s):  
G. R. Gazizova ◽  
F. V. Valeeva ◽  
M. R. Shaydullina ◽  
E. I. Akbirova

A clinical observation of a patient with Swyer's syndrome is presented. The article presents anamnesis data, phenotypic signs, clinical symptoms and objective data of the patient, the results of instrumental and hormonal studies, on the basis of which doctors of different specialties may suspect a violation of sex formation with XY gonadal dysgenesis.


2021 ◽  
Vol 34 (6) ◽  
pp. 771-772 ◽  
Author(s):  
Mary E. Fallat ◽  
Paige Hertweck ◽  
Sigal Klipstein

1979 ◽  
Vol 53 (1) ◽  
pp. 51-56 ◽  
Author(s):  
C. A. Moreira-Filho ◽  
S. P. A. Toledo ◽  
V. R. Bagnolli ◽  
O. Frota-Pessoa ◽  
H. Bisi ◽  
...  

2005 ◽  
Vol 84 (1) ◽  
pp. 217.e5-217.e6 ◽  
Author(s):  
Mei-Jou Chen ◽  
Jehn-Hsiahn Yang ◽  
Tusi-Lien Mao ◽  
Hong-Nerng Ho ◽  
Yu-Shih Yang

2018 ◽  
Vol 2 (3) ◽  
pp. 120-123
Author(s):  
Ceren SANCAR ◽  
Nuri YILDIRIM ◽  
Sevinj MAMMADOVA ◽  
Ahmet Mete ERGENOĞLU ◽  
Nedim KARADADAŞ

Sign in / Sign up

Export Citation Format

Share Document