Pulmonary alveolar proteinosis (PAP) in idiopathic hypoparathyroidism

Idiopathic hypoparathyroidism (IH) and autoimmune pulmonary alveolar proteinosis (PAP) are rare disorders. A patient with IH and optimal calcaemic control on calcium and alfacalcidol was detected to have PAP after 8 years of follow-up. Patient had no respiratory complaints. Routine abdominal imaging...

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Detaylı Bibliyografya
Yayımlandı:BMJ Case Rep
Asıl Yazarlar: Saha, Soma, Madan, Karan, Jain, Deepali, Goswami, Ravinder
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 2019
Konular:
Rare Disease
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6855869/
https://ncbi.nlm.nih.gov/pubmed/31712233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-231053
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