Laparoscopic Banded Sleeve Gastrectomy: Single-Center Experience with a Four-Year Follow-Up

2021 ◽  
Author(s):  
Paolo Gentileschi ◽  
Domenico Benavoli ◽  
Claudio Arcudi ◽  
Michela Campanelli ◽  
Marina Valente ◽  
...  
Keyword(s):  
Sleeve Gastrectomy ◽  
Single Center ◽  
Single Center Experience ◽  
Banded Sleeve Gastrectomy

Laparoscopic Sleeve Gastrectomy Versus Laparoscopic Roux-en-Y Gastric Bypass: A Single Center Experience with 2 Years Follow-Up

2014 ◽  
Vol 25 (2) ◽  
pp. 254-262 ◽  
Author(s):  
Maher El Chaar ◽  
Nadine Hammoud ◽  
George Ezeji ◽  
Leonardo Claros ◽  
Maureen Miletics ◽  
...  
Keyword(s):  
Gastric Bypass ◽  
Sleeve Gastrectomy ◽  
Laparoscopic Sleeve Gastrectomy ◽  
Single Center ◽  
Single Center Experience

Results following laparoscopic sleeve gastrectomy in elderly obese patients: a single center experience with follow-up at three years

2020 ◽  
Vol 75 (2) ◽  
Author(s):  
Paolo Bianco ◽  
Antonia Rizzuto ◽  
Nunzio Velotti ◽  
Alessio Bocchetti ◽  
Domenico Manzolillo ◽  
...  
Keyword(s):  
Sleeve Gastrectomy ◽  
Laparoscopic Sleeve Gastrectomy ◽  
Obese Patients ◽  
Single Center ◽  
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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