| Literature DB >> 15027668 |
Abstract
Surfactant Protein B (SP-B) deficiency has been recently identified as an uncommon, autosomal recessive lung disorder in term infants. This inability to produce SP-B leads to progressive, lethal, hypoxemic respiratory failure in the first year of life. A frameshift mutation (121 ins 2) is the predominant but not exclusive cause. The clue to diagnosis is to have a high suspicion of SP-B deficiency in any term infant with severe respiratory distress without any apparent cause. SP-B deficiency can be diagnosed prenatally or postnatally. The only current treatment options available include lung transplantation or compassionate care. Current developments in gene therapy offer hope for future treatment.Entities:
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Year: 2004 PMID: 15027668 DOI: 10.1097/00005237-200401000-00006
Source DB: PubMed Journal: J Perinat Neonatal Nurs ISSN: 0893-2190 Impact factor: 1.638