Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome

2004 ◽  
Vol 24 (11) ◽  
pp. 913-917 ◽  
Author(s):  
V. Satre ◽  
N. Monnier ◽  
F. Devillard ◽  
F. Amblard ◽  
Pr J. Lunardi
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome ◽  
Female Foetus

Prenatal Diagnosis and Management of Monozygotic Twins Discordant for Turner Syndrome

2013 ◽  
Vol 36 (3) ◽  
pp. 255-258 ◽  
Author(s):  
Chenyu Gou ◽  
Yu Gao ◽  
Baojiang Chen ◽  
Qun Fang
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome ◽  
Monozygotic Twins ◽  
Diagnosis And Management

Prenatal diagnosis of Turner syndrome: two clinical cases and a retrospective analysis of detected cases on the basis of the Stavropol Regional Clinical Consulting and Diagnostic Center from 2008 to 2018

2018 ◽  
Author(s):  
V.V. Ezhova, T.M. Vdovina
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome ◽  
First Trimester ◽  
Diagnostic Value ◽  
Second Trimester ◽  
Monosomy X ◽  
Clinical Observations ◽  
Diagnostic Center ◽  
Cytogenetic Studies ◽  
Full Form

Objective. The frequency of monosomy X is estimated. The diagnostic value of various ultrasound markers in a fetus with Turner syndrome in the first and second trimesters of pregnancy was evaluated. Materials. The database of cytogenetic studies from 2008 to 2018 of our center was analysed. Studies include invasive prenatal diagnosis and research on abortion material. Two clinical observations of Turner's syndrome identified in the second trimester of pregnancy were considered. Results. Of 3450 cytogenetic studies, 70 karyotypes of monosomy X were detected, the full form was found in 57 (81 %) cases, mosaic — 13 (19 %). The 46 karyotypes of monosomy X were non-developing pregnancies and 24 cases of invasive prenatal diagnosis. In the group of non-developing pregnancies, the complete form of monosomy X was observed in 40 (86.9 %) cases, mosaic — in 6 (13.1 %), embryo death in 73 % of cases occurred in the period of 8–9 weeks of gestation. The data of two clinical observations of Turner syndrome identified in the second trimester are presented. The finding ultrasonic markers of monosomy X in the analysed studies are considered. Conclusion. The detection of monosomy X is possible in most cases in the first trimester. However, the variability of symptoms and their severity does not always allow identify this pathology in the early stages. The search for soft markers during the second trimester ultrasound, the widespread use of echocardiography and a comprehensive assessment of all the studies performed can increase the frequency of detection of Turner syndrome.

PRENATAL DIAGNOSIS OF INTRACARDIAC HAMARTOMA AND TURNER SYNDROME

2010 ◽  
Vol 29 (5) ◽  
pp. 330-337 ◽  
Author(s):  
Ali Gedikbasi ◽  
Kazim Oztarhan ◽  
Kanay Yararbas ◽  
Oguz Arslan ◽  
Dogukan Yildirim ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome

Prenatal Diagnosis of Turner Syndrome

2006 ◽  
Vol 25 (6) ◽  
pp. 711-717 ◽  
Author(s):  
Csaba Papp ◽  
Artur Beke ◽  
Gabor Mezei ◽  
Zsanett Szigeti ◽  
Zoltán Bán ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome

scholarly journals Prenatal diagnosis of the Turner syndrome: what to tell the parents.

BMJ ◽  
1986 ◽  
Vol 293 (6549) ◽  
pp. 711-712 ◽  
Author(s):  
J M Connor
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome

scholarly journals Sonographic Prenatal Diagnosis of Turner Syndrome

2014 ◽  
Vol 31 (2) ◽  
pp. 99-102 ◽  
Author(s):  
Brooke Polivka ◽  
Kelsy L. Merideth
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome

Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling

2002 ◽  
Vol 22 (8) ◽  
pp. 697-702 ◽  
Author(s):  
B. Gilbert ◽  
C. Yardin ◽  
S. Briault ◽  
V. Belin ◽  
A. Lienhardt ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Turner Syndrome ◽  
Genetic Counselling ◽  
Monozygotic Twins
Sign in / Sign up

Export Citation Format

Share Document