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Pulmonary Alveolar Microlithiasis: A Review of a Rare Disease Through Rarely Discussed Perspectives.

Seminars in respiratory and critical care medicine - 1 Aug 2026

Altınışık Göksel, Yiğit Nilüfer, Çetin Nazlı

Abstract excerpt

Abstract: Pulmonary alveolar microlithiasis (PAM) has been well characterized in terms of its description, genetic background, and diagnostic process for decades; however, no effective prevention or treatment has yet been established. PAM is classified as an ultrarare lung disease linked to mutations in the autosomal recessive sodium-phosphate co-transporter gene SLC34A2, which may serve as a potential target for...

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Source

Identifiers

PMID: 41161329
DOI: 10.1055/a-2716-4930

Genes

PAM
SLC34A2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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