Ungalunyanga njani utshintsho olwenziwe yi-Beckwith-Wiedemann syndrome

Umxholo

• Uxilongo lwe-Beckwith-Wiedemann syndrome

Unyango lwe-Beckwith-Wiedemann syndrome, esisifo esinqabileyo sokuzalwa esibangela ukwanda kwamanye amalungu omzimba okanye amalungu, siyahluka ngotshintsho olwenziwe sesi sifo kwaye, ke, unyango luhlala lukhokelwa liqela elivela kubasebenzi bezempilo abaliqela. Ingabandakanya ugqirha wabantwana, ugqirha wezentliziyo, ugqirha wamazinyo kunye noogqirha abaliqela, umzekelo.

Ke, kuxhomekeke kwiimpawu kunye nokungalunganga okubangelwa yi-Beckwith-Wiedemann syndrome, ezona ntlobo zonyango ziphambili zezi:

• Ukunciphisa amanqanaba eswekile yegazi: Inaliti yeserum eneswekile yenziwa ngokuthe ngqo emthanjeni kunye nokuthintela ukungabikho kweswekile ekubangeleni utshintsho olukhulu lwe-neurological;
• I-umbilical okanye inguinal hernias: unyango alunyanzelekanga ukuba luyimfuneko njengoko uninzi lwe-hernias lunyamalala kunyaka wokuqala wobomi, nangona kunjalo, ukuba i-hernia iyaqhubeka nokwanda kubungakanani okanye ukuba ayipheli de kube yiminyaka emi-3 ubudala, kunokuba yimfuneko ukwenza utyando;
• Ulwimi olukhulu kakhulu: utyando lunokusetyenziselwa ukulungisa ubungakanani bolwimi, nangona kunjalo, kufuneka lwenziwe kuphela emva kweminyaka emi-2 ubudala. Ukuza kuthi ga kuloo minyaka, ungasebenzisa ezinye iingono ze-silicone ukunceda umntwana wakho atye ngokulula;
• Iingxaki zentliziyo okanye zesisu: amayeza asetyenziselwa ukunyanga uhlobo ngalunye lwengxaki kwaye kufuneka asetyenziswe kubomi bonke. Kwiimeko ezinzima kakhulu, ugqirha unokucebisa ukwenza utyando ukulungisa utshintsho olukhulu entliziyweni, umzekelo.

Ukongeza, iintsana ezizalwe zinesifo i-Beckwith-Wiedemann syndrome zinokuba nomhlaza, ke ukuba ukukhula kwe-tumor kuchongiwe, kusenokufuneka kwenziwe utyando ukuze kususwe iiseli zesisu okanye ezinye iindlela zonyango ezinje nge-chemotherapy okanye unyango ngemitha.

Nangona kunjalo, emva konyango, uninzi lweentsana ezine-Beckwith-Wiedemann syndrome zikhula ngendlela eqhelekileyo, ngaphandle kwengxaki ebudaleni.

Uxilongo lwe-Beckwith-Wiedemann syndrome

Ukuxilongwa kwe-Beckwith-Wiedemann syndrome kunokwenziwa kuphela ngokujonga ukungalunganga emva kokuba umntwana ezelwe okanye ngovavanyo lokuqonda isifo, njengesisu esiswini, umzekelo.

Ukongeza, ukuqinisekisa ukuxilongwa, ugqirha unokuyalela uvavanyo lwegazi ukuze enze uvavanyo lwemfuza kwaye avavanye ukuba ngaba lukhona utshintsho kwi-chromosome 11, kuba le yingxaki yemfuza ekwimvelaphi yesifo.

Isifo i-Beckwith-Wiedemann syndrome sinokudlula ukusuka kubazali siye ebantwaneni, ke ukuba nawuphi na umzali unesi sifo eselusana, ingcebiso ngofuzo iyacetyiswa ngaphambi kokuba ukhulelwe.