| Literature DB >> 28888561 |
Juan A López-Andreu1, Antonio D Hidalgo-Santos2, Miguel A Fuentes-Castelló3, Nuria Mancheño-Franch4, Juan A Cerón-Pérez5, Maria J Esteban-Ricós6, Laia Pedrola-Vidal5, Lawrence M Nogee7.
Abstract
Surfactant protein B encoding gene mutations have been related to early onset fatal respiratory distress in full-term neonates. We report a school-aged male child homozygous for a surfactant protein B encoding gene missense mutation who presented after the neonatal period. His respiratory insufficiency responded to high dose intravenous methylprednisolone and hydroxychloroquine.Entities:
Keywords: SFTPB mutation; SP-B deficiency; case report; child; corticosteroids
Mesh:
Substances:
Year: 2017 PMID: 28888561 DOI: 10.1016/j.jpeds.2017.07.009
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406