Background Poland syndrome (OMIM: 173800) is a disorder in which affected individuals are born with missing or underdeveloped muscles on one side of the body, resulting in abnormalities that can affect the chest, breast, shoulder, arm, and hand. The extent and severity of the abnormalities vary among affected individuals. Main body The aim of this work is to provide recommendations for the diagnosis and management of people affected by Poland syndrome based on evidence from literature and experience of health professionals from different medical backgrounds who have followed for several years affected subjects. The literature search was performed in the second half of 2019. Original papers, meta-analyses, reviews, books and guidelines were reviewed and final recommendations were reached by consensus. Conclusion Being Poland syndrome a rare syndrome most recommendations here presented are good clinical practice based on the consensus of the participant experts.

Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) / Baldelli, Ilaria; Baccarani, Alessio; Barone, Chiara; Bedeschi, Francesca; Bianca, Sebastiano; Calabrese, Olga; Castori, Marco; Catena, Nunzio; Corain, Massimo; Costanzo, Sara; Barbato, Giacomo De Paoli; De Stefano, Santa; Divizia, Maria Teresa; Feletti, Francesco; Formica, Matteo; Lando, Mario; Lerone, Margherita; Lorenzetti, Fulvio; Martinoli, Carlo; Mellini, Lorenzo; Nava, Maurizio Bruno; Porcellini, Giuseppe; Puliti, Aldamaria; Romanini, Maria Victoria; Rondoni, Franco; Santi, Pierluigi; Sartini, Silvana; Senes, Filippo; Spada, Lucia; Tarani, Luigi; Valle, Maura; Venturino, Cristina; Zaottini, Federico; Torre, Michele; Crimi, Marco. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 201:15(2020), pp. 1-17. [10.1186/s13023-020-01481-x]

Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence)

Baldelli, Ilaria;Castori, Marco;Costanzo, Sara;Lando, Mario;Sartini, Silvana;Tarani, Luigi;
2020

Abstract

Background Poland syndrome (OMIM: 173800) is a disorder in which affected individuals are born with missing or underdeveloped muscles on one side of the body, resulting in abnormalities that can affect the chest, breast, shoulder, arm, and hand. The extent and severity of the abnormalities vary among affected individuals. Main body The aim of this work is to provide recommendations for the diagnosis and management of people affected by Poland syndrome based on evidence from literature and experience of health professionals from different medical backgrounds who have followed for several years affected subjects. The literature search was performed in the second half of 2019. Original papers, meta-analyses, reviews, books and guidelines were reviewed and final recommendations were reached by consensus. Conclusion Being Poland syndrome a rare syndrome most recommendations here presented are good clinical practice based on the consensus of the participant experts.
2020
best practice recommendations; clinical management; diagnosis; poland syndrome; rare diseases
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) / Baldelli, Ilaria; Baccarani, Alessio; Barone, Chiara; Bedeschi, Francesca; Bianca, Sebastiano; Calabrese, Olga; Castori, Marco; Catena, Nunzio; Corain, Massimo; Costanzo, Sara; Barbato, Giacomo De Paoli; De Stefano, Santa; Divizia, Maria Teresa; Feletti, Francesco; Formica, Matteo; Lando, Mario; Lerone, Margherita; Lorenzetti, Fulvio; Martinoli, Carlo; Mellini, Lorenzo; Nava, Maurizio Bruno; Porcellini, Giuseppe; Puliti, Aldamaria; Romanini, Maria Victoria; Rondoni, Franco; Santi, Pierluigi; Sartini, Silvana; Senes, Filippo; Spada, Lucia; Tarani, Luigi; Valle, Maura; Venturino, Cristina; Zaottini, Federico; Torre, Michele; Crimi, Marco. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 201:15(2020), pp. 1-17. [10.1186/s13023-020-01481-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1680002
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