{"id":13424,"date":"2024-08-22T23:46:57","date_gmt":"2024-08-22T21:46:57","guid":{"rendered":"https:\/\/valintermed.com\/?p=13424"},"modified":"2024-08-22T23:46:57","modified_gmt":"2024-08-22T21:46:57","slug":"tyazhelyy-kombinirovannyy-immunodefitsit-stseplennyy-s-h-hromosomoy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/thiazolinone-combined-immunodeficiency-of-the-chromosomal-system\/","title":{"rendered":"X-linked severe combined immunodeficiency"},"content":{"rendered":"
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X-linked severe combined immunodeficiency (X-linked SCID) is a rare inherited disorder characterized by dysfunction of cellular and humoral immunity, resulting in increased susceptibility to infections, including those that are difficult to control and often fatal. This pathology is most often diagnosed in boys, since the mutation that causes X-linked SCID is localized on the X chromosome. The disease manifests itself early in life - in the first months or years, and is characterized by various clinical manifestations, including severe infections, some of which may be caused by common pathogens that do not cause disease in healthy people.<\/p>\n

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