Atypical hemolytic-uremic syndrome, manifesting without thrombocytopenia (clinical case)
Background. Atypical hemolytic uremic syndrome is an ultra-rare (orphan) disease from the group of thrombotic microangiopathies of progressive course, which is caused by uncontrolled activation of the alternative complement pathway of hereditary or acquired nature, leading to generalized thrombus...
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| Главные авторы: | , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Penza State University Publishing House
2024-09-01
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| Серии: | Известия высших учебных заведений. Поволжский регион: Медицинские науки |
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