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Es wird über ein frühgeborenes Mädchen berichtet, das als Kollodiumbaby auf die Welt gekommen ist. In diesem Fall beruhte der Phänotyp auf dem Krankheitsbild einer kongenitalen ichthyosiformen Erythrodermie, die durch 2 compound-heterozygote Mutationen im ALOX12B-Gen bedingt war. Unter intensiver Hautpflege, Isolierung im Inkubator mit hoher Luftfeuchtigkeit und in keimarmer Umgebung zur Infektionsprophylaxe...
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