RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164079202 T1 Morgagni-Stewart-Morel Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164079202 RD 2024/10/15 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.