Less common traits of this syndrome, such as cryptorchidism, inguinal hernia, anomalies of external genitalia, syringomyelia, congenital heart defects, and Juvenile Moyamoya [1,2,3,4,5,6,7], were never reported in this selected cohort with only NFIA haploinsufficiency, and they are probably caused by dosage alterations of different deleted genes. The gene discussed is NFIA; the disease is Inguinal hernia.