I-sturge-Weber syndrome yintlungu yesikhumba kunye nenkqubo yesifo. Uphawu lwaso olubonakalayo lubomvu oluqaqambileyo kwibala lokuzalwa elibomvu elibomvu ebusweni obubizwa ngokuba yi-port stain stain. Nangona kunjalo, akubona bonke abantu abanesiphelo sewayini esisechwebeni abane-Sturge-Weber syndrome. I-sturge-Weber syndrome ikhona ngexesha lokuzalwa, kodwa ayaziwa ukuba yintoni ebangela ukuba yenzeke okanye yintoni ebonakalayo rhoqo.
Ichaphazela bonke abesilisa nabesifazane bazo zonke iintlanga.
Kukho iintlobo ezintathu ze-Sturge-Weber syndrome:
- Uhlobo I-uhlobo oluqhelekileyo, lubandakanya i-port stain stain kunye ne-angiomas yengqondo
- Uhlobo lwesi-2 - iwayini le-port kodwa akukho ngqondo yengqondo
- Uhlobo III - ingqondo ye-angioma kodwa ayikho ibala lewayini le-port
Iimpawu
Iimpawu ze-Sturge-Weber syndrome ziquka:
- Ibala lewayini lePort - Le ngqamaniso yokuzalwa ebusweni iyakwazi ukuhluka ngobukhulu, kodwa ngokuqhelekileyo igubungela ubuncinane ikhusi eliphezulu kunye nebunzi. Iyakwazi ukusuka kwi-pink eluhlaza ukuya kumbundu obomvu kwaye ibangelwa ukukhula ngokweqile kwemithambo yegazi encinci (i-capillaries) nje ngaphantsi kwesikhumba. Isango lesitya sewayini lingaba nzima ukubona kubantu abaluhlaza.
- Ukuxhatshazwa - malunga namaphesenti angama-75 ukuya kuma-90 abantu abanesifo se-Sturge-Weber, baqala ukuxhatshazwa, ngokuqhelekileyo baqala unyaka omnye ubudala. Ukutshatyalaliswa kubangelwa ukukhula ngokweqile kwemithanjeni yegazi (angioma) ebusweni bobuchopho, ngokuqhelekileyo ngasemva kweengqondo kwicala elifanayo njengenqwelomoya yewayini.
- Ubuthathaka - malunga nama-25 ukuya kuma-56 ekhulwini abantu bahlakulela ubuthathaka okanye ukulahleka kokusetyenziswa kwelinye icala lomzimba (hemiparesis), ngokubhekiselele kwicala elijongene nebala lewayini lesipoti.
- Ukulibaziseka okuphuhlisayo kunye nokulibala kwengqondo kuthintela malunga nama-50 ukuya kuma-60 ekhulwini labantu.
- Intloko
- Uxinzelelo olwandayo kwiso (i-glaucoma) - malunga neepesenti ezingama-70 zabantu bahlakulela i-glaucoma kwiso kufuphi nebala lewayini le-port.
Ukuxilongwa
Ukuxilongwa kwe-Sturge-Weber syndrome kunokucetyiswa ngobukho bebala lewayini lesiphambano ngaphezu kweliso kunye nebunzi. Ukucwaninga kwe-tomography (CT) ekhompyutheni okanye imifanekiso yokumangalisa magnetic (MRI) inokuhlolisisa ingqondo ngenxa yobukho bodwa okanye ngaphezulu kwee-angiomas, eziza kuqinisekisa ukuxilongwa. Umntwana onesifo se-Sturge-Weber uya kuba novavanyo lwe-neurological ukuze ahlole iingxaki zeengongoma zeengqondo, ezifana nokuxhatshazwa okanye ubuthathaka.
Unyango
Utyando lwe-Sturge-Weber syndrome ligxile kwiimpawu. Ukuba i-seizures iyenzeka, imishanguzo ye-carbamazepine (Tegretol), i-phenytoin (i-Dilantin), okanye i-valproic acid (i-Depakote, i-Depakene) inikwa. Amayeza asetyenziselwa ukunciphisa nokulawula i-glaucoma kunye neentloko. Unyango lwe-Laser lunokukhanyisa okanye ususe i-port yebala ekhosini. Unyango oluninzi luyafuneka.
Umthombo:
> "Yintoni i-Sturge-Weber Syndrome?" Nge-SWS / KT / PWS. Isiseko se-Sturge-Weber. 10 Meyi 2007