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Myotonic dystrophies types 1 and 2 (DM1 / DM2) are the most frequent inherited progressive, segmental progeroid, multisystemic neuromuscular diseases in adulthood. The executive impairment is one of the key disease features. The myopathic face triggers the general perception of DM1 patients being associated with a low educational level.

Ausbildung und berufliche Qualifikation von Erwachsenen mit Myotonen Dystrophien – eine fehlgeleitete Wahrnehmung durch die Facies myopathica?