Yintoni iGilber's Syndrome kwaye inyangwa njani

Umxholo

• Iimpawu ezinokwenzeka
• Uxilongo lwenziwa njani
• Unyango lwenziwa njani

IGilbert's Syndrome, ekwabizwa ngokuba kukungasebenzi kakuhle kwesibindi ngokomgaqo-siseko, sisifo semfuza esibonakala yindlala, ebangela ukuba abantu babe nolusu namthubi. Ayithathwa njengesifo esibi, kwaye ayibangeli ngxaki zempilo, kwaye, ke, umntu onesifo u-Syndrome uphila ixesha elide njengongasithwaliyo isifo kunye nomgangatho wobomi ofanayo.

Isifo sikaGilbert sixhaphake kakhulu emadodeni kwaye sibangelwa lutshintsho kwimfuza enoxanduva lokuthotywa kwe-bilirubin, oko kukuthi, ngokutshintsha kwemfuza, i-bilirubin ayinakuthotywa, iqokelelene egazini kwaye iphuhlise imeko etyheli ephawuleka kwesi sifo .

Iimpawu ezinokwenzeka

Ngokwesiqhelo, iGilbert's Syndrome ayibangeli zimpawu ngaphandle kobukho be-jaundice, ehambelana nolusu namehlo atyheli. Nangona kunjalo, abanye abantu abanesifo baxela ukudinwa, isiyezi, intloko ebuhlungu, isicaphucaphu, urhudo okanye ukuqhina, kwaye ezi zimpawu azibonakalisi sifo. Zihlala zivela xa umntu onesifo sikaGilbert esosulelekile okanye efumana imeko yoxinzelelo olukhulu.

Uxilongo lwenziwa njani

Isifo sikaGilbert akukho lula ukusixilonga, njengoko ihlala ingenazimpawu kwaye i-jaundice inokuchazwa njengophawu lwe-anemia. Ukongeza, esi sifo, nokuba sineminyaka emingaphi, sihlala sibonisa kuphela ngamaxesha oxinzelelo, imithambo enzima, ukuzila ukutya ixesha elide, ngexesha lokugula okuthile okanye ngexesha lokuya exesheni kwabasetyhini.

Ukuxilongwa kwenzelwa ukukhuphela ngaphandle ezinye izizathu zokungasebenzi kwesibindi kwaye, ke ngoko, iimvavanyo ezingafunekiyo zovavanyo lwesibindi, ezinje nge-TGO okanye i-ALT, i-TGP okanye i-AST, kunye namanqanaba e-bilirubin, ukongeza kuvavanyo lomchamo, ukuvavanya uxinzelelo lwe-urobilinogen, igazi ukubala kwaye, ngokuxhomekeke kwisiphumo, kuvavanyo lweemolekyuli ukukhangela utshintsho olwenziwe sisifo. Jonga ukuba zeziphi iimvavanyo ezivavanya isibindi.

Ngokwesiqhelo iziphumo zovavanyo lwesibindi kubantu abane-Gilbert's Syndrome ziqhelekile, ngaphandle koxinzelelo lwe-bilirubin engathanga ngqo, engaphezulu kwe-2.5mg / dL, xa eqhelekileyo iphakathi kwe-0.2 kunye ne-0.7mg / dL. Qonda ukuba yintoni ngokuthe ngqo nangokungathanga ngqo i-bilirubin.

Ukongeza kwiimviwo ezicelwe yi-hepatologist, izinto zomzimba zomntu ziyavavanywa, ukongeza kwimbali yosapho, kuba sisifo semfuza nesaselifa.

Unyango lwenziwa njani

Akukho lunyango lonyango lwesi sifo, nangona kunjalo kufuneka ezinye izilumkiso, kuba ezinye iziyobisi ezisetyenziselwa ukulwa nezinye izifo zisenokunganyangeki esibindini, njengoko zinciphisile umsebenzi we-enzyme onoxanduva lwe-metabolism yezi ziyobisi, Umzekelo i-Irinotecan kunye ne-Indinavir, eyi-anticancer kunye ne-antiviral ngokwahlukeneyo.

Ukongeza, iziselo ezinxilisayo azikhuthazwa kubantu abane-Gilbert's syndrome, kuba kunokubakho ukonakala kwesibindi okusisigxina kwaye kukhokelele ekuqhubekeni kwesifo kunye nokuvela kwezifo ezimbi kakhulu.