PTCH1 and nevoid basal cell carcinoma syndrome: The PTCH1 gene encodes the patched‐1 receptor protein, which prevents uncontrolled cell proliferation in early development [27], and germline variants have been linked to Gorlin syndrome (high risk of basal cell carcinoma); however, at present, the PTCH1H739F variant detected here is classified as a VUS or likely benign.