Yini iGilber's Syndrome nokuthi ilashwa kanjani
-Delile
IGilbert's Syndrome, eyaziwa nangokuthi ukungasebenzi kwesibindi ngokomthethosisekelo, yisifo sofuzo esibonakala nge-jaundice, esidala ukuthi abantu babe nesikhumba namehlo aphuzi. Asibhekwa njengesifo esibi, futhi asibangeli izinkinga ezinkulu zempilo, ngakho-ke, umuntu one-Syndrome uphila isikhathi eside njengomuntu ongasithwali lesi sifo futhi enekhwalithi efanayo yokuphila.
Isifo sikaGilbert sivame kakhulu kwabesilisa futhi sidalwa yizinguquko kwisakhi esibhekele ukwehliswa kwe-bilirubin, okungukuthi, ngokuguquka kofuzo, i-bilirubin ayinakululazeka, iqoqane egazini futhi ithuthukise isici esiphuzi esiveza lesi sifo .
Izimpawu ezingenzeka
Ngokuvamile, iGilbert's Syndrome ayibangeli zimpawu ngaphandle kokuba khona kwe-jaundice, ehambelana nesikhumba namehlo aphuzi. Kodwa-ke, abanye abantu abanalesi sifo babika ukukhathala, isiyezi, ikhanda elibuhlungu, isicanucanu, isifo sohudo noma ukuqunjelwa, futhi lezi zimpawu azizona izimpawu zesifo. Imvamisa zivela lapho umuntu onesifo sikaGilbert enesifo noma ebhekene nesimo esicindezela kakhulu.
Ukuxilongwa kwenziwa kanjani
I-Gilbert's syndrome akulula ukuyithola, ngoba imvamisa ayinazo izimpawu futhi i-jaundice ingahunyushwa kaningi njengophawu lwe-anemia. Ngaphezu kwalokho, lesi sifo, kungakhathalekile ukuthi sineminyaka emingaki, sivame ukubonakala kuphela ngezikhathi zokuxineka, ukuzivocavoca umzimba okukhulu, ukuzila ukudla isikhathi eside, ngesikhathi sokugula okuthile okungahambi kahle noma ngesikhathi sokuya esikhathini kwabesifazane.
Ukuxilongwa kwenziwa ukuze kukhishwe ezinye izimbangela zokungasebenzi kahle kwesibindi, ngakho-ke, ukuhlolwa okungacelwanga kokuhlolwa kokusebenza kwesibindi, njenge-TGO noma i-ALT, i-TGP noma i-AST, namazinga e-bilirubin, ngaphezu kokuhlolwa komchamo, ukuhlola i-urobilinogen yegazi, igazi count futhi, ngokuya ngomphumela, ukuhlolwa kwamangqamuzana ukucinga ukuguquka komzimba okubangela lesi sifo. Bona ukuthi yiziphi izivivinyo ezihlola isibindi.
Imvamisa imiphumela yokuhlolwa kokusebenza kwesibindi kubantu abane-Gilbert's Syndrome ijwayelekile, ngaphandle kokuhlushwa okungaqondile kwe-bilirubin, okungaphezulu kwe-2.5mg / dL, lapho okujwayelekile kuphakathi kuka-0.2 no-0.7mg / dL. Qonda ukuthi iyini i-bilirubin eqondile nengaqondile.
Ngaphezu kwezivivinyo ezicelwe yi-hepatologist, izici zomzimba zomuntu nazo ziyahlolwa, ngaphezu komlando womndeni, ngoba kuyisifo sofuzo nesofuzo.
Yelashwa kanjani
Akukho ukwelashwa okuqondile kwalesi sifo, kepha -ke ezinye izindlela zokuqapha ziyadingeka, njengoba ezinye izidakamizwa ezisetshenziselwa ukulwa nezinye izifo zingahle zingasetshenziswa esibindini, njengoba zinciphise umsebenzi we-enzyme obhekene nokwakheka kwalezi zidakamizwa, njenge isibonelo i-Irinotecan ne-Indinavir, eyi-anticancer kanye ne-antiviral ngokulandelana.
Ngaphezu kwalokho, iziphuzo ezidakayo azinconyelwa abantu abane-Gilbert's syndrome, ngoba kungenzeka kube nokulimala kwesibindi unomphela futhi kuholele ekuqhubekeni kwesifo nasekutholakaleni kwezifo ezimbi kakhulu.