Pulmonary alveolar microlithiasis: A case report with a novel mutation in the SLC34A2 gene and review of the literature

Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive genetic disease characterized by intraalveolar psammomatous calcium phosphate deposition. Patients with PAM are often asymptomatic until the third or fourth decade, when they most frequently develop symptoms including dyspnea, and...

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Bibliographische Detailangaben
Hauptverfasser: Caroline T. Simon, MD, Toby C. Lewis, MD, MPH, Fatima Neemuchwala, MD, Manuel Arteta, MD, Raja Rabah, MD
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2018-09-01
Schriftenreihe:Human Pathology: Case Reports
Online Zugang:http://www.sciencedirect.com/science/article/pii/S221433001830004X
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