Neurocutaneous syndromes and hemangomas encompass a substantial number of
congenital or hereditary disorders, and present themselves through variable
clinical features. Though often complex and multi-systemic, these disorders can
mostly be diagnosed by simple visual inspections and strong clinical expertise.
The purpose of this book was to compile in a single volume a comprehensive
review of the historical perspective, the clinical features, the current
knowledge concerning the pathogenesis of each disease, and the diagnostic and
therapeutic strategies associated with these challenging disorders. In
particular, there is a strong emphasis throughout on the biochemical, molecular,
and genetic basis of these syndromes. The international editorial team have
drawn upon contributions from colleagues,