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Hintergrund Die Neurofibromatose Typ 1 (NF1) ist eine häufige autosomal-dominant erbliche neuroektodermale Erkrankung. Die Diagnose wird nach den NIH-Konsensus-Kriterien von 1987 gestellt. Bei Kindern gestaltet sie sich schwierig, da sich einzelne Merkmale erst entwickeln. Patienten und Methoden 28 Patienten mit NF1 im Alter von 6 Monaten–17 Jahren wurden über 7 Jahre nachuntersucht. Dokumentiert...
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