CHRONIC NEUTROPENIA REVEALING HYPER IGM SYNDROME: A CASE REPORT
- Pediatrics Department, Mohammed V Military Instruction Hospital, Rabat.
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Hyper IgM syndrome is a well-knownhereditaryimmunodeficiency, first describedin 1961. It iscaused by a defect in B lymphocytes, characterized by a normal or high serumlevel of IgM and a low or zerolevel of IgG, IgA, IgE resultingfrom a deficiency in isotype switching. Itsclinical manifestations are dominated by recurrent infections, especiallyrespiratory and digestive. The interest of this article is to illustrate a particular mode of revelation of hyper IgM syndromes through persistent chronicneutropenia in an infant.
E. Bahous, R. Abilkassem, A. Radi, M. Kmari, A. Hassani and A. Agadr (2024); CHRONIC NEUTROPENIA REVEALING HYPER IGM SYNDROME: A CASE REPORT, Int. J. of Adv. Res., 12 (12), 912-915, ISSN 2320-5407. DOI URL: https://dx.doi.org/10.21474/IJAR01/20098
pedtarics
Morocco
