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Syndrome in Question()
Immunoglobulin light chain amyloidosis is the most common acquired systemic amyloidosis. Its presentation is often insidious and progressive, which may delay diagnosis. The authors describe a rare case of immunoglobulin light chain amyloidosis in a 34-year-old man with scleroderma-like manifestation...
Kaydedildi:
| Yayımlandı: | An Bras Dermatol |
|---|---|
| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Sociedade Brasileira de Dermatologia
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4371684/ https://ncbi.nlm.nih.gov/pubmed/25831005 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20153320 |
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