| Autor: |
Thaivalappil, Silpa S., Garrod, Andrea S., Borowitz, Stephen M., Watkin, Levi B., Lawrence, Monica G. |
| Předmět: |
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| Zdroj: |
Journal of Clinical Immunology; 2021, Vol. 41 Issue 1, p205-208, 4p |
| Abstrakt: |
To the Editor: COPA syndrome is a recently described monogenic immunodysregulatory syndrome. The most common clinical features of COPA syndrome are pulmonary hemorrhage, interstitial lung disease, arthritis, glomerular disease, and autoantibody development [[2]]. We present a case of a 2-year-old male with COPA syndrome manifesting as lymphocytic interstitial pneumonitis, peripheral blood B cell lymphocytosis, mediastinal lymphadenopathy and persistent, unexplained transaminitis. [Extracted from the article] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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