Novel IL2RG gene mutation causing primary combined immunodeficiency disease: A case report and literature review
This study presents a detailed clinical case of a 10-year-old boy with a history of prolonged cough, fever, and delayed diagnosis of bronchiectasis. Review of the case revealed that the child has had recurrent bronchitis, otitis media, skin allergies, and viral warts since early childhood, indicatin...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Termedia Publishing House
2024-09-01
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| Series: | Central European Journal of Immunology |
| Subjects: | |
| Online Access: | https://www.termedia.pl/Novel-IL2RG-gene-mutation-causing-primary-combined-immunodeficiency-disease-A-case-report-and-literature-review,10,54632,1,1.html |
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