Abstract
Neural cutaneous syndromes constitute a rather heterogeneous group from a clinical standpoint. They include several distinct forms that have in common developmental anomalies of neural and other ectodermal structures; in particular, the brain, the skin, and the retina. In many of these syndromes, also known as phakomatoses and ectodermal dysplasias, visceral abnormalities are associated as well.1
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Rocco, C.D. (1992). Sturge-Weber Disease. In: Raimondi, A.J., Choux, M., Di Rocco, C. (eds) Cerebrovascular Diseases in Children. Principles of Pediatric Neurosurgery. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-2800-4_13
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