A novel combination of mutations leading to congenital ichthyosis and ichthyosis vulgaris

Abstract

Coexistence of TGM1 and FLG mutations in a newborn with congenital ichthyosis is not well described in the literature. Early genetic testing and counseling are crucial for accurate diagnosis and appropriate management. Further exploration of associated problems, including hearing loss and developmental delay, is warranted in patients with these mutations.

Keywords: dermatology; genetics; pediatrics and adolescent medicine.