Das Autoimmun-Polyendocrinopathie-Syndrom 3 ist eine familiär auftretende Erkrankung die mit verschiedenen Loci assoziiert werden konnte, deren genauer genetischer Hintergrund jedoch noch nicht ausreichend molekulargenetisch gesichert werden konnte. Der Typ 3 ist durch eine Autoimmun-Thyreoiditis und eine weitere Autoimmunerkrankung, die aber keine Nebenniereninsuffizienz sein darf, charakterisiert.
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