TY - CHAP M1 - Book, Section TI - Elejalde Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an extremely rare inherited disorder characterized by metallic silvery hair color, moderate pigment abnormalities of the skin, and early-onset profound primary central nervous system dysfunctions. Elejalde Syndrome manifests during infancy. The onset of the neurologic signs has been reported between 1 month and 11 years of age. The neurological features include severe developmental delay, seizure activity, exotropia, nystagmus, and ataxia. In comparison with the Griscelli Syndrome Type II and Chediak-Higashi Syndrome, individual affected with Elejalde Syndrome do not present immune system dysfunctions (see below). SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/14 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164068830 ER -