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

• Κύριοι συγγραφείς: Caroline T. Simon, MD (Συγγραφέας), Toby C. Lewis, MD, MPH (Συγγραφέας), Fatima Neemuchwala, MD (Συγγραφέας), Manuel Arteta, MD (Συγγραφέας), Raja Rabah, MD (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Elsevier, 2018-09-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: 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...