Bradyarrhythmias in Repaired Atrioventricular Septal Defects: Single-Center Experience Based on 34 Years of Follow-Up of 522 Patients

2018 ◽  
Vol 39 (8) ◽  
pp. 1590-1597 ◽  
Author(s):  
Corrado Di Mambro ◽  
Camilla Calvieri ◽  
Massimo Stefano Silvetti ◽  
Ilaria Tamburri ◽  
Salvatore Giannico ◽  
...  
Keyword(s):  
Single Center ◽  
Atrioventricular Septal Defects ◽  
Septal Defects ◽  
Single Center Experience

Repair of Partial Atrioventricular Septal Defects in Adults: A Single Center Experience

2020 ◽  
Author(s):  
Sri Harsha Patlolla ◽  
Joseph A. Dearani ◽  
Heidi M. Connolly ◽  
Carole A. Warnes ◽  
Brian D. Lahr ◽  
...  
Keyword(s):  
Single Center ◽  
Atrioventricular Septal Defects ◽  
Septal Defects ◽  
Single Center Experience

Early-Mid Term Follow-Up Results of Percutaneous Closure of the Interatrial Septal Defects with Occlutech Figulla Devices: A Single Center Experience

2012 ◽  
Vol 25 (4) ◽  
pp. 375-381 ◽  
Author(s):  
KUDRET AYTEMIR ◽  
ALI OTO ◽  
SÜHEYLA ÖZKUTLU ◽  
ERGÜN BARIŞ KAYA ◽  
UĞUR CANPOLAT ◽  
...  
Keyword(s):  
Percutaneous Closure ◽  
Single Center ◽  
Septal Defects ◽  
Single Center Experience

Results after repair of partial atrio-ventricular septal defects: A 50-year single-center experience

2011 ◽  
Vol 59 (S 01) ◽  
Author(s):  
A Neagoie ◽  
G Aleksieva ◽  
R Sodian ◽  
W Schiller ◽  
R Kozlik-Feldmann ◽  
...  
Keyword(s):  
Single Center ◽  
Ventricular Septal Defects ◽  
Septal Defects ◽  
Single Center Experience

scholarly journals Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey

2021 ◽  
pp. 1-6
Author(s):  
Rabia Miray Kisla Ekinci ◽  
Sibel Balci ◽  
Haldun Dogan ◽  
Serdar Ceylaner ◽  
Celal Varan ◽  
...  
Keyword(s):  
Juvenile Idiopathic Arthritis ◽  
Pericardial Effusion ◽  
Early Onset ◽  
Joint Space ◽  
Coxa Vara ◽  
Single Center ◽  
The Third ◽  
Single Center Experience ◽  
Southern Turkey

Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome, caused by biallelic pathogenic mutations in the <i>PRG4</i> gene, is characterized by early-onset camptodactyly, noninflammatory arthropathy, coxa vara deformity, and rarely, pericardial effusion. Herein, we report 3 patients with CACP syndrome from 2 unrelated families. All patients are female, born to consanguineous parents, and had camptodactyly since the first years of their lives. Two patients had a prior diagnosis of juvenile idiopathic arthritis. Hip changes were present in 2 patients, and 2 of 3 patients had undergone surgery for camptodactyly. Routine echocardiographic evaluations were normal during the 2-year follow-up. This paper represents the third study including CACP patients from Turkey. Clinically, all 3 patients resembled juvenile idiopathic arthritis cases and received unnecessary medication. There is also an ongoing need for improving awareness of CACP and an effective treatment focusing on the lubrication of the joint space in CACP patients.

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