Identification of NSDHL Mutations Associated with CHILD Syndrome in Oral Verruciform Xanthoma

To perform a systematic analysis of the NAD(P)-dependent steroid dehydrogenase-like (NSDHL) gene in cases of oral verruciform xanthoma (VX) and test for the presence of mutations associated with Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects (CHILD) Syndrome patients.

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