Alveolar proteinosis of genetic origins

Pulmonary alveolar proteinosis (PAP) is a rare form of chronic interstitial lung disease, characterised by the intra-alveolar accumulation of lipoproteinaceous material. Numerous conditions can lead to its development. Whereas the autoimmune type is the main cause in adults, genetic defects account for a large part of cases in infants and children. Even if associated extra-respiratory signs may guide the clinician during diagnostic work-up, next-generation sequencing panels represent an efficient diagnostic tool. Exome sequencing also allowed the discovery of new variants and genes involved in PAP. The aim of this article is to summarise our current knowledge of genetic causes of PAP.

Source: European Respiratory Review - October 28, 2020 Category: Respiratory Medicine Authors: Hadchouel, A., Drummond, D., Abou Taam, R., Lebourgeois, M., Delacourt, C., de Blic, J. Tags: Interstitial and orphan lung disease Rare genetic interstitial lung diseases Source Type: research