Iimpendulo zemibuzo ehlala ibuzwa malunga namaTshaba alahlekileyo
Kwiminyaka yakutshanje, ukusetyenziswa okuphezulu kwe-ultrasound ekuqaleni kokukhulelwa kuye kwandisa ubukhulu bokuxilongwa kwe-twin pregnancy , kwaye ngelishwa, kuye kwavelisa ulwazi oluphakamileyo lwe- Vanishing Twin Syndrome (VTS). Nazi iimpendulo zeemibuzo ebuzwa ngokuphindaphindiweyo malunga nale meko.
Yintoni eLahla iTwin Syndrome?
I-Vanishing Twin Syndrome ivela xa enye ye-twin ye-fetus ibonakala isuka kwisibeleko ngexesha lokukhulelwa, ngokuqhelekileyo kubangelwa ukukhulelwa okuqhelekileyo.
Yintoni eyenzeka ngokwenene?
Enye yeemfesane ekukhulelweni kwamawele ngamabini, ngokuqhelekileyo ngekota yokuqala; iisisu zomntwana zifakwe enye iwele, i-placenta, okanye umama, ngaloo ndlela unikezela ukuba iwele "yaphela."
Kufunyanwa njani?
Nantsi imeko efana neyo: Umama uhamba nge-ultrasound ekuqaleni kokukhulelwa kwakhe, umzekelo kwiinyanga ezintandathu okanye kwiiveki ezisixhenxe. Ubumbele obini bufunyanwa. Umama uxelwa ukuba unamawele.
Xa umama ebuya kumgqirha ezintandathu emva kweeveki kamva, intliziyo enye kuphela inokuvakala nge-Doppler scan. Enye i-ultrasound iyenziwa. Umntwana omnye ubonwa.
Kwamanye amaxesha, umama okhulelweyo ufumana iimpawu ezibonakala ngathi zilinganisa ukuhamba komzimba; nangona kunjalo umntwana osweleyo esibelethweni sakhe akahlali engathinteki.
Kwenzeka kaninzi?
Iingcali zenzululwazi ziqinisekisile ukuba inani lamabini amawele likhulu kakhulu kwinani lababini ababelethayo.
Olunye uqikelelo lunikela ukuba abantu aba-1 kwabangu-8 baqalise ubomi njengamawele, ngoxa kunjalo ngokwenene 1 kwi-70 ngokwenene ngamawele. Kwincwadi ethi Ukuba neentshaba (thelekisa amanani), umbhali u- Elizabeth Noble uthi ama-80% ekhulelwe ngamawele aphumela ekulahlekelweni kwesinye okanye zombini iintsana. Ezinye iziganeko ziqikelela ukuba i-Vanishing Twin Syndrome ivela kwi-21 ukuya ku-30% yazo zonke ukukhulelwa ezininzi eMelika.
Kuqikelelwa ukuba i-Vanishing Twin Syndrome iya kuba negalelo kwi-50% yokukhulelwa kwe-ovulation.
Kutheni kwenzeka njalo rhoqo?
Nangona kubonakala ngathi iziganeko ze-Vanishing Twin Syndrome zanda ngokuphindaphindiweyo, kubonakala nje ukuba ukufumanisa kwento yenyuka. Uphuhliso lwe-teknoloji ye-ultrasound luvumela oogqirha banamhlanje (kunye nabazali) ithuba elivuyisayo lokujonga kwisibeleko. Njengoko oogqirha abangakumbi basebenzisa i-ultrasound kwi-trimester yokuqala, ukukhulelwa okubanzi kubonwa. Kwaye ipesenti ethile yezo ziya kuthinteka yi-Vanishing Twin Syndrome. Kwixesha elidlulileyo, abaninzi abafazi bafumana i-VTS ngaphandle kokwazi.
Yintoni ebangela ukuba
Kanye njengoko kungekho nto ecacileyo ebangelwa ukulahleka kwezinto ezininzi, azikho izizathu okanye iinkcazo malunga nokulahlekelwa ngumntwana ekukhulelweni ezininzi. Kwezinye iimeko, umntwana ungenakwenzeka ngenxa ye-chromosomal okanye i-placental impairmentality. Ezinye iingcamango zibonisa ukuba ngenxa yokungaqhelekanga kwinto eqhelekileyo kubasetyhini abadala, i-Vanishing Twin Syndrome iqhubekile kaninzi kumama okhulileyo. I-Vanishing Twin Syndrome iyenzeka ngexesha elilinganayo kwiimbono ze-monozygotic kunye ne- dizygotic , nangona iingxaki zokwabelana nge-placenta phakathi kwamawele e-monochorionic i-monozygotic zingabangela ukuba imeko.
Ziziphi iimpawu?
Kukho akukho mpawu. Nangona kunjalo, abanye oomama banamava obunzima, ukuphaphaka okanye ukungahambi kahle kweplavic, okufana nokukhulelwa komzimba. Amanqanaba e-hormone ayancitshiswayo anokubonisa ukuba umntwana omnye uhlaziywe.
Yintoni na unyango?
Ngokuqhelekileyo, umama okanye umntwana oseleyo uya kufuna nayiphi na uhlobo lwonyango. Xa i-VTS ivela kwi-trimester yokuqala, kaninzi umama uyaqhubeka nokukhulelwa okuqhelekileyo kwaye anikezele isilwanyana esingasempilo. Nangona kunjalo, kwiimeko apho umntwana efa kwisibini okanye yesithathu, unina unokufumana umsebenzi wexesha elide, ukusuleleka okanye ukubola.
Kuloo meko, oogqirha baya kunika unyango olulungeleyo kwezo meko.
Ziziphi iinjongo zomama?
Ngokwenyama, akukho. Kodwa ngomzwelo, unina usenokuva udibaniso olungathandekiyo lweentlungu ngenxa yokulahlekelwa ngumntwana omnye kunye nokukhululeka kokusebenza komntwana osasalayo. Kubalulekile ukuba abazali baxakeke ngendlela evakalelwa ngayo, bevuma ukulahlekelwa ngumntwana kunye nokulahleka kobunikazi babo njengabazali beziphindaphindiweyo.
Ziziphi iinjongo zeewele eziphilayo?
Kwiimeko ezininzi ze-Trimester yokuLawula i-Twin Syndrome, akukho mpembelelo emzimbeni kwi-twin ehleliyo. Amava okuzaliswa kwezibeleko eziphilileyo ezilandelwa ukuhanjiswa okuqhelekileyo kufuneka kulindeleke. Ukukhulelwa kwexesha elide kwe-VTS kunempembelelo ethile kumntwana osusayo, njengokuba umama. Ngamanye amaxesha, ama-fetus atholakalayo afunyanwa kumntu osindileyo, ngendlela yesifo se-tertoma esinesithambo, iinwele, amazinyo okanye iziqwenga zenyama. Abaphandi baye bafumanisa ukuba emva kweveki ezingama-20, umntwana osasalayo unomngcipheko okhulayo wokukhubazeka kwe-cerebral palsy. Kwaye ukufa okungaqhelekanga kunokuba mngcipheko ukuba amawele angama-monozygous kwaye axelela uxhumano lwe-vascular.
Kukho ukucinga okukhulu malunga neempembelelo zengqondo kunye nemvakalelo ye-Vanishing Twin Syndrome. Abanye abasindileyo bavakalisa iimvakalelo, inecala, intlungu okanye iingxaki kunye nolwalamano okanye ubulili.
Yintoni eyenzekayo xa iwele liphela?
Ngamanye amaxesha, izilwanyana ze-fetus ezingenakulungeleka zifumaneka kumama, i-placenta okanye i-twin ephilayo. Oku kunokwenzeka ukuba kwenzeke ngekota yesithathu okanye yesithathu. Nangona ngokuqhelekileyo umntwana uya kuhlengahlengwa kwaye agcinwe, ukufa kwetawele enye kwii-15 ukuya kwiiveki ezingama-20 kunokubangela ukuba umntwana abe nepapyraceous, encinci yephepha, intsalela ye-fetal. I-tumtor ephethe i-bone, izinwele, amazinyo okanye iinqununu zesohlwayo libonisa kwakhona i-Vanishing Twin.
Singaphi na uncedo?
Iintsapho eziye zafumana i-Vanishing Twin Syndrome zingadinga ukuxhaswa kunye nokukhuthazwa ekujonganeni nelahleko ekhethekileyo. Nazi ezinye imibutho ezinokukunceda.
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I-Twwinless Twins International
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(888) 205-8962
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