# A two-month-old boy is referred for evaluation because he has an abnormal head shape. Physical examination shows low-set ears, and short-webbed fingers. A CT scan shows sagittal and lambdoid synostosis. Which of the following genes is most likely to cause this syndrome ? A. TWIST1 B. FGFR1 C. FGFR2 D. RAB23 The correct answer C. FGFR2. The most likely gene to cause the syndrome described, characterized by sagittal and lambdoid synostosis, low-set ears, and short-webbed fingers in a two-month-old boy, is C. FGFR2. Explanation: The clinical presentation suggests a craniosynostosis syndrome, with sagittal and lambdoid synostosis indicating premature fusion of cranial sutures, and additional features like low-set ears and short-webbed fingers (syndactyly) pointing toward a syndromic form. Among the options, mutations in FGFR2 (Fibroblast Growth Factor Receptor 2) are strongly associated with syndromic craniosynostoses, particularly Apert syndrome and Crouzon syndrome, both of which ...