A 12-year-old female patient (ID: 24801) with CP (*S*, LAHSHAL) and a history of intrauterine growth retardation, followed by developmental delay, expressive language delay, and behavioral issues, was found to have the variant NM_001136498.2 PCGF2 c.930dup p.(Thr311HisfsTer7), also present in her affected father. This evidence concerns the gene CP and Global developmental delay.