Prenatal diagnosis of Pfeiffer syndrome type II

2004 ◽  
Vol 24 (8) ◽  
pp. 644-646 ◽  
Author(s):  
Bettina Blaumeiser ◽  
Philip Loquet ◽  
Wim Wuyts ◽  
Markus M. Nöthen
2001 ◽  
Vol 21 (8) ◽  
pp. 565-567 ◽  
Author(s):  
Thomas E Herman ◽  
Marilyn J Siegel

1998 ◽  
Vol 13 (1) ◽  
pp. 35-38 ◽  
Author(s):  
Michael Entezami ◽  
Sanyukta Runkel ◽  
Juergen Kunze ◽  
Hans Karl Weitzel ◽  
Rolf Becker

Author(s):  
Zhi-yang Hu ◽  
Sheng Mou Lin ◽  
Meng-jie Zhu ◽  
Cindy Ka-Yee CHEUNG ◽  
Tao Liu ◽  
...  

Pfeiffer syndrome (PS) is a rare autosomal dominant genetic disorder characterized by craniosynostosis, broad thumbs / toes. Here we report a case of PS type 2 with increased nuchal translucency at early trimester.


2012 ◽  
Vol 93 (10) ◽  
pp. 785-789 ◽  
Author(s):  
H. Ben Hamouda ◽  
Y. Tlili ◽  
S. Ghanmi ◽  
H. Soua ◽  
S. Jerbi ◽  
...  

2016 ◽  
Vol 04 (03) ◽  
pp. 064-067
Author(s):  
Charanjeet Singh ◽  
Sharon Byrd ◽  
Mamta Gupta

1994 ◽  
Vol 49 (2) ◽  
pp. 240-243 ◽  
Author(s):  
Judith A. Johnson ◽  
David J. Aughton ◽  
Christine H. Comstock ◽  
Paul T. von Oeyen ◽  
James V. Higgins ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document