Fatal Familial Lung Disease Caused by ABCA3 Deficiency without Identified ABCA3 Mutations

W. Adam Gower, Susan E. Wert, Jennifer S. Ginsberg, Agneta Golan, Jeffrey A. Whitsett, Lawrence M. Nogee

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: To test the hypothesis that some functionally significant variants in the gene encoding member A3 of the ATP Binding Cassette family (ABCA3) are not detected using exon-based sequencing approaches. Study design: The first of 2 female siblings who died from neonatal respiratory failure was examined for mutations with sequence analysis of all ABCA3 exons and known regulatory elements within the 5' untranslated region. Lung tissue from both siblings was immunostained for ABCA3 and examined with electron microscopy. Segregation of ABCA3 alleles was determined with analysis of polymorphisms in the parents and all children. Results: No mutations were identified with ABCA3 sequence analysis in the first affected infant. Affected siblings were concordant for their ABCA3 alleles, but discordant from those of their unaffected siblings. ABCA3 protein was not detectable with immunostaining in lung tissue samples from both affected infants. Electron microscopy demonstrated small, dense lamellar bodies, characteristically seen with ABCA3 mutations. Conclusions: The segregation of ABCA3 alleles, absence of ABCA3 immunostaining, lung pathology, and ultrastructural findings support genetic ABCA3 deficiency as the cause of lung disease in these 2 infants, despite the lack of an identified genetic variant.

Original languageEnglish (US)
Pages (from-to)62-68
Number of pages7
JournalJournal of Pediatrics
Volume157
Issue number1
DOIs
StatePublished - Jul 2010

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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