Whole Exome Sequencing Analysis Reveals: A point mutation in the DLST Gene (c.330 + 14A>G), potentially linked to PGL Type 7, and a mutation in the Cyclin D1 (CCND1) Gene (c.575–13C>T), potentially associated with Von Hippel-Lindau Syndrome(Supplementary Table 2). This evidence concerns the gene CCND1 and von Hippel-Lindau disease.