ORIGINS AND TREATMENTS OF AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME

Authors

  • Valiyeva Nodira Andijan State Medical Institute, Uzbekistan

Keywords:

Autoimmune lymphoproliferative syndrome , lymphadenopathy, splenomegaly.

Abstract

Autoimmune lymphoproliferative syndrome is a group of genetically determined diseases that occur due to hereditary or somatic mutations in the genes responsible for various stages of FAS-related apoptosis. Symptoms can be variable and most often include lymphadenopathy, splenomegaly, and various autoimmune lesions of the blood, liver, and thyroid systems. Diagnosis of autoimmune lymphoproliferative syndrome is based on the results of general and biochemical blood tests, lymph node biopsies, and genetic studies. There is currently no specific treatment for the disease, but a combination of immunosuppressive and cytotoxic therapy is used.

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Published

2024-11-18

How to Cite

Valiyeva Nodira. (2024). ORIGINS AND TREATMENTS OF AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME. Journal of Applied Science and Social Science, 14(11), 233–236. Retrieved from https://www.internationaljournal.co.in/index.php/jasass/article/view/388

Issue

Vol. 14 No. 11 (2024): Volume 14 Issue 11

Section

Articles

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