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[Melkersson-Rosenthal syndrome in Curschmann-Steinert dystrophia myotonica]
N Stosiek1, O P Hornstein, M Meisel-Stosiek
1Dermatologische Universitätsklinik Erlangen.
Abstract:
We report the case of a 52-year-old female patient who suffered both from myotonic dystrophy (Curschmann-Steinert disease) and Melkersson-Rosenthal syndrome. Both syndromes showed the full-blown clinical features as well as the typical histology. In addition to the possibility that the appearance of the two syndromes together was a mere coincidence, we also consider the possibility that there was a hereditary diencephalic disorder present that linked together some of the minor manifestations of both syndromes.