Literature DB >> 28888561

Delayed Presentation and Prolonged Survival of a Child with Surfactant Protein B Deficiency.

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.
Copyright © 2017 Elsevier Inc. All rights reserved.

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


  4 in total

Review 1.  Genetic causes of surfactant protein abnormalities.

Authors:  Lawrence M Nogee
Journal:  Curr Opin Pediatr       Date:  2019-06       Impact factor: 2.856

2.  Difficulties in the treatment of an infant survivor with inherited surfactant protein-B deficiency in Tunisia.

Authors:  Samia Hamouda; Ines Trabelsi; Alix de Becdelièvre; Khadija Boussetta
Journal:  Ann Thorac Med       Date:  2022-04-19       Impact factor: 2.535

Review 3.  Genetic Testing for Neonatal Respiratory Disease.

Authors:  Lawrence M Nogee; Rita M Ryan
Journal:  Children (Basel)       Date:  2021-03-11

Review 4.  Childhood rare lung disease in the 21st century: "-omics" technology advances accelerating discovery.

Authors:  Timothy J Vece; Jennifer A Wambach; James S Hagood
Journal:  Pediatr Pulmonol       Date:  2020-07
  4 in total

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