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Embryology of the Neural Crest: Its Inductive Role in the Neurocutaneous Syndromes

Department of Pediatrics (Neurology), University of Calgary Faculty of Medicine and Alberta Children's Hospital, Calgary, AB, Canada, harvey.sarnat{at}calgaryhealthregion.ca, Department of Pathology (Neuropathology), University of Calgary Faculty of Medicine and Alberta Children's Hospital, Calgary, AB, Canada, Department of Clinical Neurosciences University of Calgary Faculty of Medicine and Alberta Children's Hospital, Calgary, AB, Canada

Laura Flores-Sarnat, MD

Department of Pediatrics (Neurology), University of Calgary Faculty of Medicine and Alberta Children's Hospital, Calgary, AB, Canada

Neural crest cells are first recognized at the lateral margin of the neural placode shortly after gastrulation, although they are not committed to their diverse fates until later. After dorsal closure of the neural tube, neural crest cells separate and migrate throughout the embryo to form many structures of ectodermal origin (eg, dorsal root and autonomic ganglia, peripheral nerve sheaths) and mesodermal origin (eg, blood vessels, melanocytes, adipose tissue, membranous bone, connective tissue, most of the ocular globe). Terminal differentiation occurs after migration is complete. Three regions of the neural tube generate neural crest: rhombencephalon, mesencephalon, and prosencephalon, each with a different migratory pattern. The most important genes promoting neural crest differentiation and migration are those with a dorsalizing influence in the vertical axis of the neural tube (eg, PAX3, BMP4, ZIC2), some segmentation genes (eg, WNT1), genes that inhibit neural crest (eg, EGR2), and neural crest—specific differentiating genes (eg, SLUG, SOX10). In the neurocutaneous syndromes, diverse features result from abnormal neural crest differentiation, providing a more encompassing embryologic basis for these disorders than the traditional view that these syndromes are somehow related to skin and brain because both are ectodermal derivatives. Abnormal angiogenesis, areas of abnormal pigmentation that sometimes follow the lines of Blashko, nerve sheath proliferations, disorders of chromaffin tissue, lipomes and benign and malignant tumors are frequent features. Many defective genes in neurocutaneous syndromes have an additional function as tumor suppressors. Interactions between genes associated with these disorders and others essential to neural crest formation, migration, and differentiation, are a likely molecular genetic basis for these diseases. The craniofacial abnormalities associated with many cerebral malformations and cutaneous lesions in some neurocutaneous syndromes emphasize an important inductive role of the neural tube in the development of non-neural tissues, mediated through neural crest. (J Child Neurol 2005;20:637—643).

Journal of Child Neurology, Vol. 20, No. 8, 637-643 (2005)
DOI: 10.1177/08830738050200080101


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