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12-year-old male with Elejalde syndrome (neuroectodermal melanolysosomal disease)
J Ivanovich1, S Mallory, T Storer
1Department of Pediatrics, Medical Genetics, Washington University School of Medicine, St. Louis, Missouri.
American Journal of Medical Genetics
|February 15, 2001
Abstract:
Neuroectodermal melanolysosomal disease, also known as Elejalde syndrome, is a rare syndrome characterized by silvery hair, pigment abnormalities, and profound central nervous system dysfunction. It is similar to the Chediak-Higashi and Griscelli syndromes, although these syndromes are associated with severe immunologic dysfunction. We report on a 12-year-old male with Elejalde syndrome and compare the Elejalde, Chediak-Higashi, and Griscelli syndromes.