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Etwa 1 bis 2 von 1.000 männlichen neugeborenen sind von dieser genetischen veränderung betroffen. Der zeitpunkt des auftretenden fehlers ist die reifeteilung (meiose), in deren verlauf der doppelte chromosomensatz halbiert wird. Lesen sie, welche symptome auftreten können, wie die diagnose gestellt wird und welche behandlungsmöglichkeiten es gibt. Typischerweise sind frauen mit chromosomen 46, xx und männer mit chromosomen 46, xy.
Da die krankheit im genetischen code enthalten ist, gibt es keine vollständige heilung.
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