Jacobsen’s syndrome: case report
Introduction. Jacobsen syndrome (JS) is a rare genetic disease associated with the deletion of chromosome 11q, characterized by multiple malformations, hematological and immune disorders. The development of immunodeficiency in JS is often underestimated, which leads to recurrent infectious complicat...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Russo |
| Pubblicazione: |
Association of Paediatric Allergists and Immunologists of Russia (APAIR)
2024-05-01
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| Serie: | Аллергология и Иммунология в Педиатрии |
| Soggetti: | |
| Accesso online: | https://adair.elpub.ru/jour/article/view/129 |
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