Evidence map›Paper›PMID 32758259›Full record

ReviewOrphanet journal of rare diseases2020

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

Ilaria Baldelli, Alessio Baccarani, Chiara Barone, Francesca Bedeschi, Sebastiano Bianca, Olga Calabrese, Marco Castori, Nunzio Catena, Massimo Corain, Sara Costanzo and 25 more

Open access · goldAbstract readReviewConsensus Statement
In one paragraph

Review in Orphanet journal of rare diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Reconstruction of Complex Anterior Chest Wall Defects: The Lasagna Technique.Plastic and reconstructive surgery. Global open · 2023
    Article
  14. Article
  15. Poland syndrome: Fortuitous discovery of a familial case in Togo.International journal of surgery case reports · 2023
    Article
  16. Article
  17. A de novoCold Spring Harbor molecular case studies · 2022
    Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

35 authors at 19 institutions in 2 countries.

Ilaria BaldelliPoliclinico San Martino Hospital IRCCS for Oncology, Genoa, Italy.
Alessio BaccaraniDepartment of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Modena, Italy.
Chiara BaroneMedical Genetics, Referral Centre for Rare Genetic Diseases, ARNAS Garibaldi, Catania, Italy.
Francesca BedeschiClinical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Sebastiano BiancaMedical Genetics, Referral Centre for Rare Genetic Diseases, ARNAS Garibaldi, Catania, Italy.
Olga CalabreseMedical Genetic Unit, University Hospital of Modena, Modena, Italy.
Marco CastoriDivision of Medical Genetics, Fondazione IRCCS-Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy.
Nunzio CatenaPediatric Orthopedic and Traumatology Unit Azienda Ospedalieria SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Massimo CorainHand Surgery Unit - Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Sara CostanzoPediatric Surgery Unit, V. Buzzi Children's Hospital, Milan, Italy.
Giacomo De Paoli BarbatoAzienda USL di Ferrara, Ospedale del Delta, Ferrara, Italy.
Santa De StefanoAssociazione Italiana Sindrome Poland, Via Asiago, 3r, 16137, Genoa, Italy.
Maria Teresa DiviziaMedical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Francesco FelettiDepartment of Diagnostic Imaging AUSL of Romagna, U.O. of Radiology, "Santa Maria delle Croci" Civil Hospital, Ravenna, Italy.
Matteo FormicaOrthopedic Clinic, Department of Surgical Sciences, University of Genova, Ospedale Policlinico San Martino, Genoa, Italy.
Mario LandoDepartment of Muscle-Skeletal Surgery, Hand and Microsurgery Division, Modena University Hospital, Modena, Italy.
Margherita LeroneMedical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Fulvio LorenzettiPlastic and Reconstructive Surgery Unit, University of Pisa, Santa Chiara Hospital, Pisa, Italy.
Carlo MartinoliDepartment of Health Science, Section of Radiology, University of Genoa, Genoa, Italy.
Lorenzo MelliniAssociazione Italiana Sindrome Poland, Via Asiago, 3r, 16137, Genoa, Italy.
Maurizio Bruno NavaG.Re.T.A. Group for Reconstructive and Therapeutic Advancements, University of Genoa, Genoa, Italy.
Giuseppe PorcelliniDepartment of Orthopaedics and Traumatology, Modena Policlinic, Modena, Italy.
Aldamaria PulitiMedical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Maria Victoria RomaniniPlastic and Reconstructive Surgery, Pediatric Surgery Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Franco RondoniUSL Umbria 1, Ospedale Città di Castello, Perugia, Italy.
Pierluigi SantiPoliclinico San Martino Hospital IRCCS for Oncology, Genoa, Italy.
Silvana SartiniHand Rehabilitation Center, Modena University Hospital, Modena, Italy.
Filippo SenesReconstructive Surgery and Hand Surgery Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Lucia SpadaCentro di Educazione Matrimoniale e Prematrimoniale, Genoa, Italy.
Luigi TaraniDepartment of Pediatrics, "Sapienza", University of Rome, Rome, Italy.
Maura ValleUOC Radiologia Neuroradiologia, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Cristina VenturinoPsychiatric Service, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Federico ZaottiniDepartment of Health Science, Section of Radiology, University of Genoa, Genoa, Italy.
Michele TorreAssociazione Italiana Sindrome Poland, Via Asiago, 3r, 16137, Genoa, Italy.
Marco CrimiAssociazione Italiana Sindrome Poland, Via Asiago, 3r, 16137, Genoa, Italy. mcrimi@kaleidos.care.ORCID 0000-0001-6903-9163
Istituto Giannina Gaslini · ITUniversity of Modena and Reggio Emilia · ITOspedale Policlinico San Martino · ITUniversity of Genoa · ITOspedale Garibaldi · ITAssociazione Italiana Sclerosi Multipla · ITAzienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo · ITAzienda Ospedaliera Universitaria Integrata Verona · ITAzienda Ospedaliero-Universitaria di Modena · ITAzienda Unità Sanitaria Locale di Ferrara · ITCasa Sollievo della Sofferenza · ITCittà di Castello Hospital · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITKaleida Health · USOspedale dei Bambini Vittore Buzzi · ITOspedale "Santa Maria delle Croci" di Ravenna · ITSapienza University of Rome · ITUniversity of Ferrara · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPoland 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.

conclusionBeing Poland syndrome a rare syndrome most recommendations here presented are good clinical practice based on the consensus of the participant experts.

Indexed as

Poland SyndromeHealth PersonnelHumansBest practice recommendationsClinical managementDiagnosisPoland syndromeRare diseases

Identifiers

PMID32758259
PMCPMC7405453
OpenAlexW3047099406

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.