The aim of investigation is to describe the clinical case of a patient with Wiskott-Aldrich Syndrome. Materials and methods. We present a clinical case of a boy born in 2007 with a clinical picture of primary immunodeficiency, manifested in the form of Wiskott-Aldrich Syndrome. The child is under the supervision of a hematologist and immunologist at the Center for Pediatric Hematology, Oncology and Clinical Immunology. Results and discussion. The boy had a wide range of clinical and laboratory symptoms, such as a serious condition of the child, severe intoxication, hepatosplenomegaly, petechial rashes on the skin of the body, hemorrhagic syndrome, anemia of unknown origin in the blood, leukocytosis, accelerated ESR, thrombocytopenia. Taking into account all the above indicators and data, Primary Immunodeficiency, Wiskott-Aldrich Syndrome diagnosis was established. Conclusion. Based on this clinical case, one can be convinced that the clinical picture, including the characteristic triad of symptoms of this disease, is quite specific. Consequently, it helps doctors in differential diagnosis with other diseases.
| Mualliflar | Kxanova , Kxilolakxon, Ismailova , Adolat, Ханова , Хилолахон, Исмаилова , Адолат, Xanova , Xilolaxon, Ismailova , Adolat |
|---|---|
| Jurnal | Халқаро илмий педиатрия журнали |
| Nashr sanasi | 2022-11-30 |
| Jild | 1 |
| Son | 7 |
| Betlar | 21-24 |
| Til | Rus |
| DOI | 10.56121/2181-2926-2022-7-21-24 |
DOI: 10.56121/2181-2926-2022-7-21-24 · Maqolaning asl sahifasi
Синдром Вискотта-Олдрича, врожденные ошибки иммунитета, первичный иммунодефицит, тромбоцитопения, экзема, петехии, дети, Wiskott-Aldrich syndrome, congenital immune disorders, primary immunodeficiency, thrombocytopenia, eczema, petechiae, hemorrhagic syndrome, Viskott-Aldrich sindromi, tug'ma immunitet buzilishlari, birlamchi immunitet tanqisligi, trombotsitopeniya, ekzema, petexiya, gemorragik sindrom
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