I-Patau Syndrome iyakwazi ukuxilongwa ngexesha lokukhulelwa
I-Chromosomal engafanelekanga yinto enobangela bokulahleka kwemithwalo kunye nokuzala. Ukungaqhelekanga kunokubangela imiba ebalulekileyo, kuquka i-Down Syndrome kunye nokulibaziseka kokuphuhliswa okanye imicimbi yezempilo. Kwi-trisomy, abantu banamakhophi amathathu e-chromosome ngaphezu kwezinto ezimbini eziqhelekileyo.
I-Patau syndrome, okanye i-Trisomy 13, yinto eqhelekileyo ye-autosomal trisomies kunye neyona nto inzima, emva kwe- Down syndrome (iTrisomy 21) kunye ne- Edwards syndrome (iTrisomy 18) .
Ikopi eyongezelelweyo ye-chromosome 13 kwi-Patau syndrome ibangela ukukhubazeka okukhulu kweengqondo kunye neentliziyo ezenza kube nzima ukuba iintsana ziphile. Isizathu esona sizathu sePatau syndrome asiyazi; Kuyafana ne- VATER Syndrome . I-Patau ibonakala ichaphazela amabhinqa angaphezu kwamadoda, mhlawumbi ngenxa yokuba abantwana abathandwayo abasayi kuphila kude kube sekuzalweni. I-Patau syndrome, efana ne-Down syndrome, inxulumene nokukhula komama. Inokuchaphazela abantu bazo zonke iintlanga.
Iimpawu
Iintsana ezizalwe ngePatau syndrome zidla ngokungaqhelekanga okanye imiba yengqondo. Iintsana ezininzi aziphili ngaphambili kwinyanga yokuqala okanye kunyaka wokuqala. Ezinye iimpawu ziquka:
- Iminwe eminwe okanye iinzwane (i-polydactyly)
- Iinyawo eziphosakeleyo, ezaziwa njengeenyawo eziphantsi kweenyawo
- Iingxaki ze-neurological ezifana nentloko encinci (i-microcephaly), ukungaphumeleli kwengqondo kulwahlula kwii-halves ngexesha lokugaya (holoprosencephaly), ukusilela kwengqondo
- Iziphoso ezinjengezamehlo amancinci (i-microphthalmia), iipumphu ezingekho okanye ezingenakulimala, umlomo womlomo kunye / okanye ukucoca
- Iintsilelo zeentliziyo (80% yabantu)
- Iingxaki zeentso
Ukukhula
I-Patau syndrome ayiqhelekanga; Abantwana abayi-16,000 kuphela abanesifo. I-95% yabantwana abanePatau syndrome bafa ngaphambi kokuzalwa.
Ukuxilongwa
Iimpawu zePatau syndrome zibonakala ngexesha lokuzalwa. I-Patau syndrome inokuphosakela kwi-syndrome ye-Edwards, ngoko uvavanyo lwezofuzo kufuneka lwenziwe ukuze kuqinisekiswe ukuxilongwa. Izifundo zokucinga ezifana ne- computed tomography (CT) okanye i-imagery magnetic resonance (MRI) kufuneka yenziwe ukuba ikhangele ubuchopho, intliziyo kunye neentsilelo zeentso. Kufuneka kwenziwe i-ultrasound ye-heart (echocardiogram) ngenxa yeenyawo eziphakamileyo zeentliziyo eziphene ezinxulumene nePatau syndrome.
Unyango
Ukunyangwa kwe-Patau syndrome kugxile kwiingxaki ezithile zomzimba apho umntwana ngamnye azalwa khona. Iintsana ezininzi zinenkinga yokuphila kwiintsuku ezimbalwa zokuqala okanye iiveki ngenxa yeengxaki zeengxaki ze-neurological or defective heart defects. Kufuneka ukuba unyango lukulungele ukulungisa iimpazamo zentliziyo okanye umlomo ococekileyo kunye ne-palate. Ulwaphulo lomzimba, usebenze, nolulwalathiso luya kunceda abantu abanePatau syndrome bafikelele ekuphuculeni ngokupheleleyo.
Kwenziwe ntoni
Ukuba umntwana wakho ufunyanwe ukuba une-Patau syndrome ngaphambi kokuzalwa, ugqirha wakho uya kuhamba kunye nezinto ozikhethayo. Abanye abazali bafuna ukungenelela okunzulu, kanti abanye bakhetha ukuphelisa ukukhulelwa. Abanye baya kuqhubeka nokukhulelwa baze banikele ngononophelo ngobomi bomntwana. Nangona amathuba okusinda aphantsi kakhulu, abanye abantu banquma ukuzama ukunonyamekela ukunyusa ubomi bomntwana.
Ezi zigqibo zizodwa kwaye zingenziwa kuphela kuwe, iqabane lakho kunye nodokotela wakho.
Ukululekwa nge-Genetic kunye neNkxaso
Abazali bomntwana ozalwe ngePatau syndrome baya kufumana isiluleko sofuzo ukuze baqinisekise ukuba yintoni umngcipheko wokuba nomnye umntwana one-syndrome. Uluhlu olulungileyo ngolwazi nenkxaso yiNkxaso yeNhlangano yeTrisomy 18, 13 kunye nezinye izifo ezichaphazelekayo (SOFT).
> Imithombo:
> Eyona ndawo, RG, Stallworth, J., & Dacus, JV (2002). Patau Syndrome.
> "Patau Syndrome." IThala leNcwadi kaZwelonke kwiMpilo yeGenetic, ngo-2009.