Ingaba kukho ikhonkco phakathi kwe-Iron Overload kunye ne-Hypothyroidism?

Ingqwalasela yeHeredicromatosis yeHereditary

I-hemochromatosis ye-Hereditary yintlupheko yesifo okanye ifa, esibizwa ngokuba yi- iron overload disease. Ubangelwa ukuxutywa kwinyithi eninzi emanzini akho (ukusuka kokutya) obangela isinyithi ukuba igcinwe kwizitho, njengebindi, intliziyo kunye neepakresi.

Unokumangaliswa xa ufumanisa ukuba i-thyroid ingasebenzi nayo inokubangelwa kwi- hemochromatosis . Oku kungenxa yokuba isinyithi singafakwa kwi-pituitary gland, ebangela ukuba i-hypothyroidism ephakathi, okanye ingaphantsi, i-thyroid gland, ebangela i-hypothyroidism ephambili.

Makhe sijonge ngakumbi i-hemochromatosis, kubandakanywa ukuba le mvelaphi ye-genetic ibonisa njani kwaye iyaphathwa.

Izinto zobungozi

Kukho izinto ezinobungozi bokuphuhlisa i-hemochromatosis. Ekubeni i-hemochromatosis yimiqathango yokuguqulwa kwe-autosomal, uya kufuna iikopi ezimbini zokuguqula izityalo ukuze ziphuhlise.

Ngaphezu koko, ukuba yiCaucasus yaseNyakatho yeYurophu yinto engozi. Ukongeza, ukuba yindoda inyuse amathuba okuphuhlisa i-hemochromatosis, njengoko abafazi balahlekelwa yinyithi ngokuya esikhathini, ngoko ke bayakha i-iron engaphantsi. Umngcipheko wesifazana ukhuphuka, nangona kunjalo, emva kokumisa umva , xa engasayi kukhaleni.

Izibonakaliso kunye neMpawu

Ukubonakaliswa kwe-hemochromatosis akuyi kukhula kuze kube yilapho ikhulile, kwaye kuxhomekeke kwiziphi izitho ezichaphazelekayo, umntu unokufumana iimpawu eziguqukayo. Abantu abaninzi, ngokwenene, bafumanisa ukuba bane-hemochromatosis (ngokusekelwe kwimbali yentsapho okanye ukuhlolwa kwegazi okungenakwenzeka) ngaphambi kokuba bavelise iimpawu.

Kwakhona kubalulekile ukuba uqaphele ukuba idilesi yokufakela isinyithi inokwenzeka ngaphakathi kwinqanaba ngaphandle kweembonakaliso zeklinikhi. Ngokomzekelo, izifundo ze-autopsy ziye zityhila i-iron deposits kwi-thyroid gland malunga nabo bonke abantu abane-hemochromatosis; kodwa, abaninzi abantu abane-hemochromatosis abayikuhlakulela i-hypothyroidism eyona nto (kubalulekile ukugcina engqondweni).

Kodwa ke, iimpawu eziqhelekileyo kunye neempawu ze-hemochromatosis ziquka:

Njengoko imeko iyaqhubeka, ukuba ingashiywanga, umntu unokuhlakulela:

Ukuxilongwa novavanyo

Ukuba ufumana iimpawu zentsimbi ephezulu kwaye ugqirha wakho ufumanisa amanqanaba ensimbi ephakamileyo kwigazi lakho, unokuyalela ukuba ahlolwe igazi nge-gene hemochromatosis.

Ukongezelela, ngokweSiko leSizwe soSwekile neSigestive kunye neNtsholongwane yezifo, ezi zilandelayo zikhokelo zovavanyo mazilandelwe:

Okokugqibela, ukuba uqiniseke ngokuthe ngqo ukubandakanyeka kwe-thyroid-gland kwi-hemochromatosis, i- MRI ye-thyroid gland ingakwazi ukubona i-deposit ye-iron.

Unyango

I-Hemochromatosis iphathwa ngokuthi "ukugalelwa kwegazi" okanye i-phlebotomy-ngokuyisiseko, inkqubo elula yokunika igazi. Ugqirha wakho uya kuphuhlisa ishedyuli rhoqo ye-phlebotomy, njengonyango lwe-hemochromatosis.

ILizwi

I-Hemochromatosis yisona sifo esiqhelekileyo se-genetic e-United States, kwaye iindaba ezilungileyo kukuba ukubonakaliswa kwayo okukhulu, njengobindi, intliziyo kunye nesifo se-thyroid, kunokuthintela ngokunyamekela.

Ukuba unentsapho yenkcitho yesitrity overload okanye iimpawu ezingachazwanga, kunengqiqo ukuthetha nodokotela wakho malunga nokuvavanya.

> Imithombo:

> Schrier SL, iBacon BR. (2018). Izibonakaliso zekliniki kunye nokuxilongwa kwe-hemochromatosis yefa. Ku: U-UpToDate, iMentzer WC (Ed), UpToDate, Waltham, MA.

> Tamagno G, De Carlo E, Murialdo G, Scandellari C. Unxibelelwano olunokwenzeka phakathi kwe-genetic hemochromatosis kunye ne-autoimmune thyroiditis. Minerva Med . 2007 Dec; 98 (6): 769-72.