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Ako toto ochorenie vzniká? Najčastejšie už pri počatí, dieťatko sa narodí s jedným chromozómom naviac a týmto sú tieto deti výnimočné. Existuje niekoľko presných vyšetrení, ktoré dokážu takmer so 100% presnosťou už počas tehotenstva určiť či plod je týmto ochorením postihnutý, a tak sa môžu nastávajúci rodičia na príchod bábetka pripraviť a naštudovať si to čo ich čaká dopredu.
Samozrejme niektorý rodičia zistia, že nie sú schopný sa o takto postihnuté dieťa postarať a rozhodnutú sa o umelé prerušenie tehotenstva. Z genetickej indikácie je potrat možný až do 24 týždňa gravidity, teda hmotnost dieťatka môže byť už i 400-500g!