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Hyper immunoglobulin-M Syndrome in children

عنوان مقاله: Hyper immunoglobulin-M Syndrome in children
شناسه ملی مقاله: JR_INTJMI-6-4_004
منتشر شده در شماره ۴ دوره ۶ فصل در سال 1396
مشخصات نویسندگان مقاله:

Reza Sadeghnezhad - Student of Environmental Health Engineering, Student Research Committee, Faculty of Health & Health Sciences Research Center, Mazandaran university of Medical Sciences, Sari, Iran
Mahdiye Babaei hatkehlouei - Dentistry student, Student Research Committee, Mazandaran University of Medical Science, Sari, Iran
Masoud Golpour - Associated Professor, Department of Dermatology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
Hamed Jafarpour - Medical Student, Student Research Committee, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran

خلاصه مقاله:
Introduction: Hyper immunoglobulin-M syndrome (HIGM) is a rare, x-linked recessive inherited disorder with Increased or normal serum IgM and decreased IgA, IgG and IgE and normal peripheral B cells. In this disease, we have defect in class switch recombination (CSR) and somatic hyper mutation that is caused by defects including the enzymes required for CSR and SHM. (SHM)Methods: To update about HIGM, PubMed and Google Scholar database were searched for term, X linked Hyper IgM syndrome and CD40 ligand. In our first search, we received about 90 updated articles, and then we distributed these articles among the authors. After reading the articles and sharing together, finally 33 articles were selected that fully related to the topic as references.Findings: In conclusion, HIGM is rare disease that starts early in life with lifelong recurrent attacks of various infections by a variety of symptoms, including lymph Adenopathy, vomiting, diarrhea, skin lesion and abdominal pain. Allogenic hematopoietic cell transplantation and BMT can be effective in these patients.Conclusion: In conclusion, HIGM is rare disease that starts early in life with lifelong recurrent attacks of various Infections by a variety of symptoms, including lymphadenopathy, vomiting, diarrhea, skin lesions and abdominal pain. Allogenic hematopoietic cell transplantation and BMT can be effective in these patients.

کلمات کلیدی:
CD40 ligand, X linked hyper-IgM, Immune Deficiency Syndromes

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/937146/