A Rare Autoimmune Disease Detected in the Differential Diagnosis of Immunodeficiency: Histiocytosis-lymphadenopathy Plus Syndrome
Mutations in the SLC29A3 gene cause histiocytosis-lymphadenopathy plus (H) syndrome, a rare autosomal recessive genetic condition that affects numerous systems. We present a 7-year-old Syrian patient with pericardial effusion whose acute phase reactants did not decrease despite treatment. In order...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Tehran University of Medical Sciences
2023-09-01
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| Col·lecció: | Iranian Journal of Allergy, Asthma and Immunology |
| Matèries: | |
| Accés en línia: | https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3643 |
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