Minerva Medica 2019 Jun 25

DOI: 10.23736/S0026-4806.19.06054-3

Copyright © 2019 EDIZIONI MINERVA MEDICA

lingua: Inglese

Primary ciliary dyskinesia: can we identify patients with the most severe phenotype?

Gioia PIATTI ¹, Maria Margherita DE SANTI ², Andrea FAROLFI ³, Lucia BARCELLINI ³, Enza C. D'AURIA ³, Maria Francesca PATRIA ⁴, Dario CONSONNI ⁵, Umberto AMBROSETTI ⁶ ✉

¹ Unit of Bronchopneumology, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; ² Unit of Pathological Anatomy, Department of Human Pathology and Oncology, Policlinico Le Scotte, University of Siena, Siena, Italy; ³ Department of Pediatric Pulmonology, Vittore Buzzi Children’s Hospital, University of Milan, Milan, Italy; ⁴ Paediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan, Milan, Italy; ⁵ Epidemiology Unit, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Milan, Italy; ⁶ Audiology Unit, Department of Clinical Sciences and Community Health, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, University of Milan Milan, Italy