scholarly journals EP07.05: A case of double Trisomy (T21 and T18)

2018 ◽  
Vol 52 ◽  
pp. 221-221
Author(s):  
A. Yulia ◽  
M. Vendola ◽  
R. Wimalasundera
Keyword(s):  
2005 ◽  
Vol 24 (5) ◽  
pp. 717-719 ◽  
Author(s):  
Victor Dezerega ◽  
Cecilia Be ◽  
Amy E. Wong ◽  
Rafael Silva ◽  
Waldo Sepulveda

2009 ◽  
Vol 40 (4) ◽  
pp. 215-218 ◽  
Author(s):  
Suhair S. Eid ◽  
Montaha M. Shawabkeh ◽  
Ali A. Hawamdeh ◽  
Nazmi R. Kamal

2004 ◽  
Vol 47 (1) ◽  
pp. 95-98 ◽  
Author(s):  
Dimitrios Iliopoulos ◽  
George Poultsides ◽  
Vasiliki Peristeri ◽  
Georgia Kouri ◽  
Alexandros Andreou ◽  
...  

2008 ◽  
Vol 11 (2) ◽  
pp. 147-150 ◽  
Author(s):  
John B. Mailhes ◽  
Charleen M. Moore ◽  
Juan J. Gershanik
Keyword(s):  

2018 ◽  
Vol 97 (2) ◽  
pp. 585-585
Author(s):  
Laura Daniela Vergara-Mendez ◽  
Claudia Talero-Gutiérrez ◽  
Alberto Velez-Van-Meerbeke
Keyword(s):  

1998 ◽  
Vol 179 (6) ◽  
pp. 1654 ◽  
Author(s):  
Swarna K. Gogineni ◽  
Ram S. Verma
Keyword(s):  

1997 ◽  
Vol 101 (3) ◽  
pp. 339-345 ◽  
Author(s):  
K. S. Reddy

2000 ◽  
Vol 2 (1) ◽  
pp. 91-91
Author(s):  
H B Ai-Kouatlv ◽  
C Johnson ◽  
D Skupski ◽  
M Lita Alonso

2005 ◽  
Vol 45 (1) ◽  
pp. 21-25 ◽  
Author(s):  
Qing Ying Li ◽  
Sami Tsukishiro ◽  
Chiaki Nakagawa ◽  
Mitsuyo Tanemura ◽  
Mayumi Sugiura-Ogasawara ◽  
...  

2020 ◽  
Vol 23 (5) ◽  
pp. 356-358
Author(s):  
Mahdi Bijanzadeh ◽  
Shahram Rajaei Behbahani

Double trisomy 48, XXY, +21 or Down-Klinefelter syndrome is a rare occurrence and presents clinical manifestation of trisomy 21 in early life and of Klinefelter syndrome after 10 months of age. The phenotypic and karyotyping characteristics of a 2-month-old boy were reported. He had mild clinical feature of Down syndrome and echocardiographic features of atrioventricular (AV) septal defects with severe pulmonary valve stenosis.


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