Co-Occurrence of <i>RAD21</i> and <i>TNFAIP3</i> Mutations in Cornelia de Lange Syndrome with Pustular Psoriasis: Potential Molecular Interactions.

RAD21 knockdown is associated with a trend toward reduced TNFAIP3 mRNA expression compared to control ( Figure 5 a), although this difference did not reach statistical significance.

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The co-occurrence in one individual is extremely rare and has only been reported in a handful of cases worldwide, making the present case highly significant for both clinicians and researchers [ 14 , 51 ].

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