scholarly journals F93Feasibility of the second trimester fetal ultrasound examination in an unselected population at 18, 20 or 22 weeks of pregnancy: a randomized trial

2000 ◽  
Vol 16 ◽  
pp. 57-57
Author(s):  
P. Schwärzler ◽  
Y. Ville
2006 ◽  
Vol 195 (5) ◽  
pp. 1379-1387 ◽  
Author(s):  
Patrick Rozenberg ◽  
Laurence Bussières ◽  
Sylvie Chevret ◽  
Jean Pierre Bernard ◽  
Lydia Malagrida ◽  
...  

Author(s):  
I.N. Daminov

A case of prenatal ultrasound diagnosis of fibular hemimelia, type I associated with oligodactyly of the foot at 22 weeks of gestation is presented. Ultrasound examination at 22 weeks of gestation revealed hypoplasia of the left fibula and the foot oligodactyly. After prenatal counseling, the patient opted for termination of pregnancy. During external examination of the abortus asymmetry of the lower extremities due to shortening of the left lower leg and oligodactyly of the left foot were noted, those confirmed prenatal ultrasound data.


2018 ◽  
Vol 97 (11) ◽  
pp. 1300-1308 ◽  
Author(s):  
Florent Fuchs ◽  
Julie Burlat ◽  
Fréderic Grosjean ◽  
Romy Rayssiguier ◽  
Guillaume Captier ◽  
...  

2018 ◽  
Vol 131 ◽  
pp. 183S
Author(s):  
Megan Weatherborn ◽  
Heidi Leftwich ◽  
Bailey McGuinness ◽  
Maureen Ogamba ◽  
Katherine Leung

2019 ◽  
Vol 8 (2) ◽  
Author(s):  
Giulia Garofalo ◽  
Marie Cassart ◽  
Julie Désir ◽  
Dominique Thomas

Abstract Background Prenatal diagnosis of congenital ichthyosis is still a challenge and very few cases of sonographic diagnosis have been described in the literature. Diagnosis by fetal ultrasound is made from the late second trimester and prenatal genetic diagnosis can be possible only if a proband is known. Case presentation We report the case of a prenatal diagnosis of severe non-syndromic ichthyosis in a primigravida woman with no personal or family history for this pathology. Conclusion Our case outlines prenatal sonographic signs suggestive of ichthyosis orienting genetic diagnosis.


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