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- W3048210885 abstract "Abstract Paediatric disorders of pulmonary surfactant may occur due to mutations involving surfactant proteins B and C, and ATP‐binding cassette subfamily A member 3 ( ABCA3 ) genes. Recessive frameshift or nonsense ABCA3 mutations are associated with respiratory failure and neonatal death but milder phenotypes of ABCA3 deficiency due to missense, splice site, and insertion/deletions may result in survival beyond infancy. To date, only one case report describes the clinical course from birth to age 21 years and there are less than 10 adult cases. No guidelines exist for medical therapy due to the rarity of this condition. We describe the clinical course of a patient over 39 years and her younger brother who were both diagnosed at birth with an unspecified paediatric interstitial lung disease (ILD) and were eventually diagnosed with ABCA3 mutation in their adulthood. Our report highlights the minimal progression of the ABCA3 ‐related ILD without long‐term medications, but the development of dyspnoea due to progressive pulmonary hypertension and airflow obstruction." @default.
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- W3048210885 date "2020-08-07" @default.
- W3048210885 modified "2023-10-09" @default.
- W3048210885 title "<scp> <i>ABCA3</i> </scp> deficiency from birth to adulthood presenting as paediatric interstitial lung disease" @default.
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- W3048210885 doi "https://doi.org/10.1002/rcr2.633" @default.
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