scholarly journals 22q11.2 Duplication Syndrome with Persistent 5th Aortic Arch

2019 ◽  
Vol 35 (4) ◽  
pp. 279-283
Author(s):  
Yusuke Yano ◽  
Takashi Murakami ◽  
Kazuo Imagawa ◽  
Nobuyuki Ishikawa ◽  
Yoshihiro Nozaki ◽  
...  
Author(s):  
Adam Butensky ◽  
Chiara Pandolfi Rinaldis ◽  
Shrey Patel ◽  
Sharon Edman ◽  
Alice Bailey ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
A. Bahji ◽  
S. Khalid-Khan

22q11.2 duplication syndrome is a recently discovered genetic syndrome with unclear neuropsychiatric sequelae. While its connection to 22q11.2 deletion syndrome is actively investigated, case reports on the neuropsychiatric sequelae of affected individuals have been previously described, largely focusing on comorbid autism spectrum disorder. Here, we present the case of an 8-year-old female experiencing episodes of severe behavioural regression following medical illness. We analyze the case and relate it to the available literature and identify potential risk factors.


2016 ◽  
Vol 7 (1) ◽  
Author(s):  
Tara L. Wenger ◽  
Judith S. Miller ◽  
Lauren M. DePolo ◽  
Ashley B. de Marchena ◽  
Caitlin C. Clements ◽  
...  

2016 ◽  
Vol 236 ◽  
pp. 206-207 ◽  
Author(s):  
Therese van Amelsvoort ◽  
Astrid Denayer ◽  
Jacques Boermans ◽  
Ann Swillen

2008 ◽  
Vol 51 (6) ◽  
pp. 501-510 ◽  
Author(s):  
Christian Wentzel ◽  
Maria Fernström ◽  
Ylva Öhrner ◽  
Göran Annerén ◽  
Ann-Charlotte Thuresson

2008 ◽  
Vol 4 (1) ◽  
pp. 10 ◽  
Author(s):  
Anna Brunet ◽  
Lluís Armengol ◽  
Trini Pelaez ◽  
Roser Guillamat ◽  
Vicenç Vallès ◽  
...  

2018 ◽  
Vol 27 (11) ◽  
pp. 1847-1857 ◽  
Author(s):  
Erica Hasten ◽  
Donna M McDonald-McGinn ◽  
Terrence B Crowley ◽  
Elaine Zackai ◽  
Beverly S Emanuel ◽  
...  

2005 ◽  
Vol 137A (1) ◽  
pp. 47-51 ◽  
Author(s):  
Marie-France Portnoï ◽  
Fanny Lebas ◽  
Nicolas Gruchy ◽  
Azarnouche Ardalan ◽  
Valérie Biran-Mucignat ◽  
...  

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