Ten‐year follow up of hydroxychloroquine treatment for ABCA3 deficiency
Identifieur interne : 000095 ( Istex/Curation ); précédent : 000094; suivant : 000096Ten‐year follow up of hydroxychloroquine treatment for ABCA3 deficiency
Auteurs : Michael Williamson [Royaume-Uni] ; Colin Wallis [Royaume-Uni]Source :
- Pediatric Pulmonology [ 8755-6863 ] ; 2014-03.
Abstract
We present a child with interstitial lung disease (ILD) who was diagnosed with desquamative interstitial pneumonitis following CT thorax and open lung biopsy aged 2 years. Subsequently, surfactant protein gene analysis revealed mutations in the ABCA3 gene. This case of ABCA3 deficient ILD describes a stable clinical course over 10 years and highlights the potential benefit of hydroxychloroquine for this condition. Pediatr Pulmonol. 2014; 49:299–301. © 2013 Wiley Periodicals, Inc.
Url:
DOI: 10.1002/ppul.22811
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<front><div type="abstract" xml:lang="en">We present a child with interstitial lung disease (ILD) who was diagnosed with desquamative interstitial pneumonitis following CT thorax and open lung biopsy aged 2 years. Subsequently, surfactant protein gene analysis revealed mutations in the ABCA3 gene. This case of ABCA3 deficient ILD describes a stable clinical course over 10 years and highlights the potential benefit of hydroxychloroquine for this condition. Pediatr Pulmonol. 2014; 49:299–301. © 2013 Wiley Periodicals, Inc.</div>
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