Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review

被引：0
作者：
Gloria Pelizzo
Mirella Collura
Aurora Puglisi
Maria Pia Pappalardo
Emanuele Agolini
Antonio Novelli
Maria Piccione
Caterina Cacace
Rossana Bussani
Giovanni Corsello
Valeria Calcaterra
机构：
[1] Pediatric Surgery Department,Pediatric Anesthesiology and Intensive Care Unit
[2] Children’s Hospital “G. di Cristina”,Pediatric Radiology Unit
[3] ARNAS Civico-Di Cristina-Benfratelli,Laboratory of Medical Genetics
[4] Cystic Fibrosis and Respiratory Pediatric Center,Department of Sciences for Health Promotion and Mother and Child Care “Giuseppe D’Alessandro”
[5] Children’s Hospital G. Di Cristina,Neonatal Intensive Care Unit
[6] ARNAS Civico-Di Cristina-Benfratelli,Institute of Pathological Anatomy
[7] Children’s Hospital G. Di Cristina,Pediatrics and Neonatal Intensive Therapy Unit, Mother and Child Department
[8] ARNAS Civico-Di Cristina-Benfratelli,Pediatrics and Adolescentology Unit
[9] Children’s Hospital G. Di Cristina,undefined
[10] ARNAS Civico-Di Cristina-Benfratelli,undefined
[11] Bambino Gesù Children’s Hospital,undefined
[12] University of Palermo,undefined
[13] Hospital “Barone Romeo” Patti,undefined
[14] ASP Messina,undefined
[15] Trieste University Hospital,undefined
[16] University of Palermo,undefined
[17] Department of Internal Medicine University of Pavia and Fondazione IRCCS Policlinico San Matteo,undefined
来源：
BMC Pediatrics | / 19卷
关键词：
Filamin a; Congenital enphysema; Lung disease; Children; Periventricular nodular heterotopia;
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Khong TY(2014)Filamin a mutation may be associated with diffuse lung disease mimicking bronchopulmonary dysplasia in premature newborns Respir Care 59 e171-149
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