Encephalocraniocutaneous lipomatosis is a rare congenital neurocutaneous disease that shows unilateral lipomatous skin formations on the hairless area as well as unilateral defects of the eyes and nervous system. The pathogenesis of EKL remains unclear. The clinical and morphological observation of encephalocraniocutaneous lipomatosis diagnosed at the birth of a child are provided.

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Автор(ы): M. K. Nedzvedz, S. K. Kletsky, S.A. Guzov, S. V. Viktor