JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot

2013 ◽  
Vol 161 (12) ◽  
pp. 3133-3136 ◽  
Author(s):  
Maria Cristina Digilio ◽  
Alessandro De Luca ◽  
Francesca Lepri ◽  
Valentina Guida ◽  
Rosangela Ferese ◽  
...  
Keyword(s):  
Tetralogy Of Fallot ◽  
Deletion 22Q11.2

Prenatal diagnosis of Di George syndrome of the fetus with tetralogy of Fallot

2020 ◽  
Author(s):  
O.A. Grammatikova, , G.A. Ryabchenko , A.M. Bondarev
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Prenatal Diagnosis ◽  
Tetralogy Of Fallot ◽  
Congenital Heart ◽  
Second Trimester ◽  
Deletion 22Q11.2 ◽  
Di George Syndrome

Prenatal diagnosis of deletion 22q11.2 of the fetus in the second trimester of pregnancy, suspected on the basis of congenital heart disease (tetralogy of Fallot) in the combination with thymus hypoplasia, is presented. The pregnancy was interrupted.

Surgical management of tetralogy of Fallot in the first year of life: Current indications for palliation

2004 ◽  
Vol 52 (S 1) ◽  
Author(s):  
H G�rler ◽  
A B�ning ◽  
J Scheewe ◽  
J Paulsen ◽  
HH Kramer ◽  
...  
Keyword(s):  
Tetralogy Of Fallot ◽  
Surgical Management ◽  
First Year ◽  
First Year Of Life
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