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- Kevan Mehta, Sharon Dell, Catherine Birken, and Suhail Al-Saleh.
- Hospital for Sick Children, 555 University Avenue, Toronto, ON, Canada M5G 1X8.
- Can. Respir. J. 2016 Jan 1; 2016: 4938632.
AbstractPulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive condition that is often asymptomatic despite significant changes in chest imaging. Diagnosis is often made when patients become symptomatic in adulthood. There are still no proven treatments, but earlier diagnosis may allow for evaluation of preventative strategies that could improve outcome. It is an important diagnosis to consider in children who have marked radiographic findings with no or very mild symptoms or physical findings. Diagnosis can be made with imaging alone but may necessitate lung biopsy for definitive diagnosis.
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