Ngokuvamile owesifazane okhulelwe uthunyelwa ukuhlaziywa kwe- Down's syndrome , futhi akekho umuntu ochaza ukuthi yini eyabangela lesi sidingo. Kufanele kuqaphele ukuthi ukuthuthukiswa kwemithi kusanda kuvumela uhlobo olunjalo lomcwaningi wesisu. Ngaphambilini, ukuhlolwa kuphela kwe-Down's syndrome kwenziwa, okwakubonisa izimpawu eziqondile zokuba khona kwe-fetal disease. Okwamanje, kunezindlela eziningi zokusungula ukuxilongwa okunjalo.
Ukuhlaziywa kwe-Genetic ye-Down syndrome
Inqubo yokuzala ingane encane, owesifazane ubhekene nesidingo sokuthatha inamba enkulu yokuhlolwa futhi ahambe ngezifundo eziningi. Esinye sinjalo ukuhlolwa kwegazi kwe-Down syndrome. Akufanele sishaye indiva ukubaluleka kwayo, ngoba akusiwo sonke esiwazi ukuzalwa kwethu kofuzo futhi sinomthwalo omkhulu wenhlalakahle yengane engakazalwa. Uma imiphumela yocwaningo olunjalo ayiduduza, futhi i-geneticist idinga ukubonakaliswa kwe-pathology, ngakho-ke kufanelekile ukuhlola i-Down syndrome. Kuhilela ukuqoqwa kwezinto eziphilayo zengane noma amniotic fluid ngokusebenzisa udonga lwesisu lomama kanye nesifundo sayo esilandelayo.
Ingozi ye-Down syndrome
Ithuba lokukhiqiza "ingane enelanga" likhuphuka kakhulu kubazali asebekhulile uma iminyaka yowesifazane idlulile iminyaka engama-35, kanti amadoda - 45. Futhi, amacala alesi senzakalo ayenzeka kumama omncane kakhulu, nangokwenyamazane, okungukuthi, imishado ephakathi kwezihlobo eziseduze. Akudingekile ukuxosha izakhi zofuzo zabazali kanye nesisu, isimo sengqondo sokungahloniphi ukuhlela nokukhulelwa ngesikhathi sokubeletha. Ngakho-ke, ukuhlolwa kokuhlolwa kwe-Down's syndrome kuyimpoqo. Nguye owenza kube lula ukuqinisekisa noma ukuphikisa ukutholakala kwamathologi emntwaneni bese wenza isinqumo esifanele ngesikhathi.
Kunemikhuba ethile engozini ye-Down's syndrome, enqunywa imiphumela ye-ultrasound kanye ne-correlate ngenkathi yokubeletha kanye nemingcele evunyelwe ngokuvamile yokuphambukiswa. Udokotela unesithakazelo ebude bamathambo ekhaleni kanye nobukhulu bekhala,
Down Syndrome Biochemistry Risk
Ukuhlaziywa okunjalo kusivumela ukuthi sinqume ukukhubazeka ezinkathini zokuqala zokubeletha, ngokoqobo kusuka emavikini angu-9-13. Esikhathini sokuqala, kuba khona amaprotheni othize, owesibili ulinganisa isakhi ngasinye seHCG ye-hormone nokunye. Kumele kuqashelwe ukuthi i-laboratory ngayinye ingase ibe nenqubo eyingozi yobungozi be-Down's, ngakho-ke kuyadingeka ukuthola izincazelo zemiphumela endaweni yokulethwa kokuhlaziywa.