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

• Asıl Yazarlar: Caroline T. Simon, MD (Yazar), Toby C. Lewis, MD, MPH (Yazar), Fatima Neemuchwala, MD (Yazar), Manuel Arteta, MD (Yazar), Raja Rabah, MD (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Elsevier, 2018-09-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

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...