TY - CHAP M1 - Book, Section TI - Morgagni-Stewart-Morel Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a polyglandular endocrine syndrome characterized by diabetes insipidus, mellitus, and hyperparathyroidism. Clinically, affected individual present with the classic triad of (a) hyperostosis frontalis interna, (b) adipositas, and (c) virilism and hirsutism. There is a peculiar, noninflammatory, usually benign osteopathy with symmetrical thickening of the frontal, parietal, or occipital bones as a result of deposits on the internal aspects of the squama frontalis. Other clinical features include menstrual disorders, galactorrhea, mental dysfunctions, fatigue, somnolence, visual disorders, vertigo, tinnitus, obesity, polyphagia, polydipsia, polyuria, loss of sense of smell, decreased glucose tolerance, seizures, and involvement of the second, fifth, and seventh cranial nerves with hemiplegia and hemiparesis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164079202 ER -