Clinical, histological, and ultrasound follow-up of breast reconstruction with one-stage muscle-sparing “wrap” technique: A single-center experience

2017 ◽  
Vol 70 (11) ◽  
pp. 1527-1536 ◽  
Author(s):  
Maria Giuseppina Onesti ◽  
Michele Maruccia ◽  
Giuseppe Di Taranto ◽  
Antonio Albano ◽  
Giuseppe Soda ◽  
...  
2021 ◽  
pp. 1-6
Author(s):  
Rabia Miray Kisla Ekinci ◽  
Sibel Balci ◽  
Haldun Dogan ◽  
Serdar Ceylaner ◽  
Celal Varan ◽  
...  

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.


Hernia ◽  
2004 ◽  
Vol 8 (4) ◽  
pp. 350-353 ◽  
Author(s):  
L. M. Veenendaal ◽  
G. J. de Borst ◽  
P. H. P. Davids ◽  
G. J. Clevers

Pituitary ◽  
2011 ◽  
Vol 15 (1) ◽  
pp. 25-29 ◽  
Author(s):  
Panagiotis Anagnostis ◽  
Fotini Adamidou ◽  
Stergios A. Polyzos ◽  
Zoe Efstathiadou ◽  
Eleni Karathanassi ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document