NEUROCUTANEOUS SYNDROMES IN CHILDREN -- Contents -- Chapter 1 - Embryological basis of the neurocutaneous syndromes -- Chapter 2 - Neurocutaneous diseases in children and adolescents: general clinical pattern -- Chapter 3 - Hypomelanosis of Ito -- Chapter 4 - Vascular malformations and neurocutaneous disorders -- Chapter 5 - Neurocutaneous syndromes and hemimegalencephaly -- Chapter 6 - Two rare neurocutaneous syndromes: Wyburn-Mason and Proteus -- Chapter 7 - Diagnostic criteria and evaluation of patients with tuberous sclerosis complex -- Chapter 8 - Epileptic manifestations in tuberous sclerosis -- Chapter 9 - Tuberous sclerosis complex: phenotype-genotype correlations -- Chapter 10 - Subependymal giant cell astrocytomas and tuberous sclerosis -- Chapter 11 - Neurosurgical strategies in the management of subependymal giant cell tumoursin tuberous sclerosis complex -- Chapter 12 - The neurofibromatoses: clinical manifestations, natural history and management -- Chapter 13 - Neurofibromatosis type 1: the dermatological option -- Chapter 14 - Clinical molecular genetics of the neurofibromatoses -- Chapter 15 - Cognitive-behavioural phenotype and neurobiological basis of neurofibromatosis type 1 -- Chapter 16 - Brain tumours in neurofibromatosis type 1 -- Chapter 17 - Novel therapeutic approaches for plexiform neurofibromas in neurofibromatosis type 1 -- Chapter 18 - Adjuvant therapy for low-grade glioma in neurofibromatosis type 1 -- Chapter 19 - Diagnostic and follow-up protocols for neurofibromatosis types 1 and 2.