Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome
Congenital defects of the sternum are rare and due to a failure of midline development and fusion of the sternal bones. Surgical correction of a sternal cleft should be preferred during infancy for functional reasons. Chest wall reconstruction represented a complex problem in the last decades.
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De Gruyter
2016-01-01
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doaj-16cf15f2d7074960be8951411201bc9c2021-10-02T02:55:05ZengDe GruyterOpen Medicine2391-54632016-01-0111119619910.1515/med-2016-0037med-2016-0037Sternal reconstruction by extracellular matrix: a rare case of phaces syndromeMolinaro Francesco0Garzi Alfredo1Cerchia Elisa2Di Crescenzo Vincenzo Giuseppe3Luzzi Luca4Bulotta Anna Lavinia5Gotti Giuseppe6Messina Mario7Division of Pediatric Surgery, Department of Medical, Surgical and Neurological Sciences, University of Siena, ItalyUniversity Salerno, Salerno, ItalyDepartment of Medical, Surgical and Neurological Science. Pediatric Surgery Unit, University of Siena, ItalyDepartment of Medicine and Surgery, Thoracic Surgery Unit, University of Salerno, ItalyThoracic Surgery Unit, University Hospital of Siena, Siena, ItalyDepartment of Medical, Surgical and Neurological Science. Pediatric Surgery Unit, University of Siena, ItalyThoracic Surgery Unit, University Hospital of Siena, Siena, ItalyDepartment of Medical, Surgical and Neurological Science. Pediatric Surgery Unit, University of Siena, ItalyCongenital defects of the sternum are rare and due to a failure of midline development and fusion of the sternal bones. Surgical correction of a sternal cleft should be preferred during infancy for functional reasons. Chest wall reconstruction represented a complex problem in the last decades.http://www.degruyter.com/view/j/med.2016.11.issue-1/med-2016-0037/med-2016-0037.xml?format=INTPhaces syndromeSternal reconstructionMidline development defects |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Molinaro Francesco Garzi Alfredo Cerchia Elisa Di Crescenzo Vincenzo Giuseppe Luzzi Luca Bulotta Anna Lavinia Gotti Giuseppe Messina Mario |
spellingShingle |
Molinaro Francesco Garzi Alfredo Cerchia Elisa Di Crescenzo Vincenzo Giuseppe Luzzi Luca Bulotta Anna Lavinia Gotti Giuseppe Messina Mario Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome Open Medicine Phaces syndrome Sternal reconstruction Midline development defects |
author_facet |
Molinaro Francesco Garzi Alfredo Cerchia Elisa Di Crescenzo Vincenzo Giuseppe Luzzi Luca Bulotta Anna Lavinia Gotti Giuseppe Messina Mario |
author_sort |
Molinaro Francesco |
title |
Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome |
title_short |
Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome |
title_full |
Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome |
title_fullStr |
Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome |
title_full_unstemmed |
Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome |
title_sort |
sternal reconstruction by extracellular matrix: a rare case of phaces syndrome |
publisher |
De Gruyter |
series |
Open Medicine |
issn |
2391-5463 |
publishDate |
2016-01-01 |
description |
Congenital defects of the sternum are rare and due to a failure of midline development and fusion of the sternal bones. Surgical correction of a sternal cleft should be preferred during infancy for functional reasons. Chest wall reconstruction represented a complex problem in the last decades. |
topic |
Phaces syndrome Sternal reconstruction Midline development defects |
url |
http://www.degruyter.com/view/j/med.2016.11.issue-1/med-2016-0037/med-2016-0037.xml?format=INT |
work_keys_str_mv |
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