Quick Search:

uzh logo
Browse by:
bullet
bullet
bullet
bullet

Zurich Open Repository and Archive

Koller, M F; Papassotiropoulos, A; Henke, K; Behrends, B; Noda, S; Kratzer, A; Hock, C; Hofmann, M (2005). Evidence of a genetic basis of Morgagni-Stewart-Morel syndrome. A case report of identical twins. Neuro-degenerative Diseases, 2(2):56-60.

Full text not available from this repository.

View at publisher

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.

Citations

2 citations in Web of Science®
6 citations in Scopus®
Google Scholar™

Altmetrics

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Psychiatric University Hospital Zurich > Division of Psychiatric Research and Clinic for Psychogeriatric Medicine
DDC:610 Medicine & health
Language:English
Date:2005
Deposited On:09 Sep 2011 14:18
Last Modified:28 Oct 2014 16:01
Publisher:Karger
ISSN:1660-2854
Publisher DOI:10.1159/000089284
PubMed ID:16909048

Users (please log in): suggest update or correction for this item

Repository Staff Only: item control page