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Autor:
Emad Alkhankan, MD, Hasan Yamin, MD, Hazim Bukamur, MD, Fadi Alkhankan, MD, Yousef Shweihat, MD, Fuad Zeid, MD
Publikováno v:
Radiology Case Reports, Vol 14, Iss 6, Pp 775-777 (2019)
Pulmonary alveolar microlithiasis is rare disease characterized by accumulation of calcium phosphate microlithis in the alveoli. The pathogenesis relates to mutation in the gene SLC34A2 (solute carrier family 34 member 2) located on chromosome 4p15.2
Externí odkaz:
https://doaj.org/article/ad2358552e3b45e4b4f1e3b8bd3abd36