The 22q11 microdeletion syndrome in children

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Abstract

DiGeorge syndrome is a primary immunodeficiency with microdeletion 22q11. Prenatal diagnosis is possible. Typical disorders are heart defects of heart and large vessels, hypoplasia of the parathyroid glands, dysmorphia, no thymus and immune deficiency. The primary problem is the heart defect requiring cardiac surgical intervention. Due to the severity of the operation, immunodeficiency often goes into the background. Infections are associated with cardiovascular abnormalities. The immune deficit is omitted without proper treatment including isolation of the patient, substitution of i.v. immunoglobulin, chemo-prophylaxis. Blood products must be irradiated. What should be applied is oncology alertness and limitation of X-ray should also be noted. A comprehensive care reduces infections and improves the quality of life.

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Lewandowicz-Uszyńska, A., Zwonarz, K., & Chmielarska, J. (2013). The 22q11 microdeletion syndrome in children. Central-European Journal of Immunology. Termedia Publishing House Ltd. https://doi.org/10.5114/ceji.2013.35220

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