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Pulmonary alveolar microlithiasis: no longer in the stone age
Pulmonary alveolar microlithiasis (PAM) is a rare parenchymal lung disease caused by variants in the SCL34A2 gene and characterised by the accumulation of intra-alveolar microliths. PAM has been reported in fewer than 1100 cases throughout the world. It is an autosomal recessive hereditary disease a...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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European Respiratory Society
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487355/ https://www.ncbi.nlm.nih.gov/pubmed/32964001 http://dx.doi.org/10.1183/23120541.00289-2020 |