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Evidence of a Genetic Basis of Morgagni-Stewart-Morel Syndrome.

Authors :
Koller, Michael F.
Papassotiropoulos, Andreas
Henke, Katharina
Behrends, Britta
Noda, Shigeru
Kratzer, Adelgunde
Hock, Christoph
Hofmann, Marc
Source :
Neurodegenerative Diseases. 2005, Vol. 2 Issue 2, p56-60. 5p. 4 Diagrams, 1 Chart.
Publication Year :
2005

Abstract

We report two 71-year-old female monozygotic twins presenting with advanced hyperostosis frontalis interna, obesity, shortness and cognitive impairment. They both have suffered from generalized seizures since their early adulthood. Moreover, the patients showed some additional conditions only occurring in one individual or the other such as migraine, marked recurrent depressive disorder or polyarthrosis. The symptoms common to both twins appear to correspond to the Morgagni-Stewart-Morel syndrome and indicate a genetic basis of this disorder as these features occur in genetically identical patients. Copyright © 2005 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16602854
Volume :
2
Issue :
2
Database :
Academic Search Index
Journal :
Neurodegenerative Diseases
Publication Type :
Academic Journal
Accession number :
19889901
Full Text :
https://doi.org/10.1159/000089284