Ukuya ocansini kwengane: kuyini, ukukwenza nini nemiphumela

-Delile

• Kwenziwa kanjani ukuhlolwa
• Intengo yokuhlolwa kwezocansi kwe-Fetal
• Ungayihumusha kanjani imiphumela

Ukuya ocansini kwengane ukuhlolwa okuhlose ukukhomba ubulili bengane kusukela ngesonto lesi-8 lokukhulelwa ngokuhlaziywa kwegazi likamama, lapho kuqinisekiswa khona ukutholakala kwe-Y chromosome, ekhona kwabesilisa.

Lokhu kuhlolwa kungenziwa kusukela ngeviki lesi-8 lokukhulelwa, kepha-ke uma uthola amasonto amaningi okukhulelwa, ukuqiniseka komphumela kukhula kakhulu. Ukwenza lokhu kuhlola, owesifazane okhulelwe akadingi ukwelulekwa ngudokotela futhi akumele azile ukudla, kubalulekile ngisho ukuthi adliswe kahle futhi anikwe amanzi ukuze angabi nokugula ngesikhathi sokuqoqa.

Kwenziwa kanjani ukuhlolwa

Ukuhlolwa kobulili embungwini kwenziwa ngokuhlaziya isampula legazi elincane elithathwa kowesifazane, bese lithunyelwa elabhorethri liyohlolwa. Kulebhu, kuhlolwa izingcezu ze-DNA ezivela embungwini osegazini likamama, bese kwenziwa ucwaningo kusetshenziswa izindlela zamangqamuzana, njenge-PCR, ukuthola ukuthi ubukhona noma ukungabikho kwesifunda se-SYR, okuyi isifunda esiqukethe i-chromosome Y, ekhona kubafana.

Kunconywa ukuthi ukuhlolwa kwenziwe kusukela ngeviki lesi-8 lokukhulelwa ukuze uqiniseke ngokwengeziwe ngomphumela. Kodwa-ke, abesifazane abaye bafakelwa umnkantsha wamathambo noma ukumpontshelwa igazi umnikeli wabo ungowesilisa akufanele benze ucansi lwengane, ngoba umphumela kungenzeka ukuthi awulungile.

Intengo yokuhlolwa kwezocansi kwe-Fetal

Intengo yokuya ocansini kwengane iyahlukahluka kuye ngelabhorethri lapho kwenziwa khona ukuhlolwa nokuthi uma kukhona ukuphuthuma kokuthola imiphumela yokuhlolwa, kubiza kakhulu kulezi zimo. Isivivinyo asitholakali kwinethiwekhi yomphakathi futhi asikhokhelwa ngezinhlelo zezempilo kanye nezindleko eziphakathi kuka-R $ 200 no-R $ 500.00.

Ungayihumusha kanjani imiphumela

Umphumela wokuhlolwa kwezocansi kombungu uthatha cishe izinsuku eziyi-10 ukuthi ukhishwe, kepha uma ucelwa ngokushesha, umphumela ungakhishwa kuze kufike ezinsukwini ezi-3.

Isivivinyo sihlose ukukhomba ubukhona noma ukungabi bikho kwesifunda se-SYR, okuyisifunda esiqukethe i-chromosome Y. Ngakho-ke, imiphumela emibili engenzeka yokuhlolwa yilena:

• Ukungabikho kwesifunda se-SYR, okukhombisa ukuthi ayikho i-chromosome Y, ngakho-ke, iyi- intombazane;
• Ubukhona besifunda se-SYR, okukhombisa ukuthi iyi-Y chromosome futhi, ngakho-ke, iyi- umfana.

Endabeni yokukhulelwa amawele, uma umphumela ungathandeki ku-Y chromosome, umama uzokwazi ukuthi ukhulelwe amantombazane kuphela. Kepha, uma umphumela ulungile ku-Y chromosome, lokhu kukhombisa ukuthi kukhona okungenani umfana oyedwa, kepha lokho akusho ukuthi enye ingane nayo.