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Article

Pulmonary Alveolar Microlithiasis.

Clinics in chest medicine - 1 Sept 2016

Saito Atsushi, McCormack Francis X

Abstract excerpt

Pulmonary alveolar microlithiasis (PAM) is a genetic lung disorder that is characterized by the accumulation of calcium phosphate deposits in the alveolar spaces of the lung. Mutations in the type II sodium phosphate cotransporter, NPT2b, have been reported in patients with PAM. PAM progresses gradually, often producing incremental dyspnea on exertion, desaturation in young adulthood, and respiratory...

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Identifiers

PMID: 27514591
DOI: 10.1016/j.ccm.2016.04.007
PMCID: PMC4987712

Genes

PAM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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