Literature DB >> 16909048

Evidence of a genetic basis of Morgagni-Stewart-Morel syndrome. A case report of identical twins.

Michael F Koller1, Andreas Papassotiropoulos, Katharina Henke, Britta Behrends, Shigeru Noda, Adelgunde Kratzer, Christoph Hock, Marc Hofmann.   

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.

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Year:  2005        PMID: 16909048     DOI: 10.1159/000089284

Source DB:  PubMed          Journal:  Neurodegener Dis        ISSN: 1660-2854            Impact factor:   2.977


  3 in total

1.  Frontal cortex dysfunction due to extensive hyperostosis frontalis interna.

Authors:  Thomas Gilbert; Sabrina Ait; Floriane Delphin; Emmanuel Raharisondraibe; Marc Bonnefoy
Journal:  BMJ Case Rep       Date:  2012-01-10

2.  Frequency of hyperostosis frontalis interna in patients with active acromegaly: is there a possible role of GH excess or hyperprolactinemia in its etiopathogenesis?

Authors:  Ummu Mutlu; Ozge Telci Caklili; Mehmet Barburoglu; Sema Yarman
Journal:  Hormones (Athens)       Date:  2022-10-12       Impact factor: 3.419

3.  A Case Report of Hyperostosis Frontalis Interna.

Authors:  Luis A Alvarez; William Corrigan; Seth Gardner
Journal:  Cureus       Date:  2022-05-13
  3 in total

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