Blink-Stuart-Morel syndrome
- Authors: Ismagilov M.F.1, Khasanova D.R.1, Galimullina Z.A.1, Sharayienidze D.M.1
-
Affiliations:
- Imperial Kazan University
- Issue: Vol XXVI, No 3-4 (1994)
- Pages: 72-76
- Section: Reviews
- URL: https://journals.rcsi.science/1027-4898/article/view/107191
- DOI: https://doi.org/10.17816/nb107191
- ID: 107191
Cite item
Full Text
Abstract
The Morgagni-Stewart-Morel syndrome (frontal hyperostosis syndrome, metabolic craniopathy) according to the classical description includes a triad of symptoms: thickening of the internal plate of the frontal bone, obesity and virilism.
In 1762, Morgagni, opening the corpse of a 40-year-old woman, established a thickening of the inner plate of the frontal bone, and at the same time excessive obesity and male-type hairiness. He considered these signs not coexisting, but interconnected and described this observation.
Keywords
Full Text
##article.viewOnOriginalSite##About the authors
M. F. Ismagilov
Imperial Kazan University
Author for correspondence.
Email: info@eco-vector.com
Professor, Head of the Department of Neuropathology, Neurosurgery and Medical Genetics
Russian Federation, KazanD. R. Khasanova
Imperial Kazan University
Email: info@eco-vector.com
Department of Neuropathology, Neurosurgery and Medical Genetics
Russian Federation, KazanZ. A. Galimullina
Imperial Kazan University
Email: info@eco-vector.com
Department of Neuropathology, Neurosurgery and Medical Genetics
Russian Federation, KazanD. M. Sharayienidze
Imperial Kazan University
Email: info@eco-vector.com
Department of Neuropathology, Neurosurgery and Medical Genetics
Russian Federation, Kazan