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Atypical Omenn Syndrome due to Adenosine Deaminase DeficiencyDOI: 10.1155/2012/919241 Abstract: We present here a novel case of an atypical Omenn syndrome (OS) phenotype due to mutations in the ADA gene encoding adenosine deaminase. This case is noteworthy for a significant increase in circulating CD56brightCD16- cytokine-producing NK cells after treatment with steroids for skin rash.
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