Xa i-Anemia ye-Arsenal iyakwazi ukuba yintoni?

Ngamanye amaxesha, izigulane ezine- anemia ezingenasitya aziphendulanga kwisinyithi. Ezi zi gulane zingaba zongezelelwe ngeesinyithi kwiinyanga ukuya kwiminyaka zingenakuphucula ukuphulelwa kwegazi. Izizathu zokuthi kungani isiguli singaphenduli kwiyeza zentsimbi ziquka:

Thalassemia Trait

I-Thalassemia ithetha igazi elwandle njengoko lidibene neLwandle iMeditera. Namhlanje i-thalassemia ibonakala kumaqela amaninzi nakwiintlanga. I-Thalassemia yintlupheko ye-hemoglobin, iprotheni kwiiseli ezibomvu zegazi.

Oku kubangela i-anemia elula kunye neeseli ezincinci zegazi ezibomvu (ezibizwa ngokuba yi-microcytosis). Abantu abathwala i-thalassemia (ebizwa ngokuba yi-thalassemia trait) bangakhohliswa njenge-anemia ye-iron. Kukho iintlobo ezimbini ezibalulekileyo ze-thalassemia, i-alpha kunye ne-beta.

Isizathu sokuba abantu abaneThalassemia Trait Get Mislabeled as Anemia Deficiency Anemia

Ixabiso lebhu ibonakala kakhulu kwi-iron deficiency kunye ne-thalassemia. Ekugqibeleni kokuqala kwegazi elipheleleyo (iCBC), i-hemoglobin iya kuba sezantsi ibonisa i- anemia kunye nomlinganiselo we-corpuscular volume (MCV), okanye ubungakanani belifom yegazi elibomvu, liya kuba sezantsi. Uninzi lwabantu abanolu tshintsho kwi-CBC banesifo se-anemia.

Ukuvavanya ukusilela kwesinyithi kunokunyaniseka. Izinga lensimbi lithonyelwa kukutya. Ukuba isigulane sinamabhanki atyelela into yokuqala ekuseni, ngaphambi kokuba anento yokutya, inqanaba lesinyithi linokuba liphantsi ngenxa yokuba akazange athengise nantoni ngensimbi. Uvavanyo olungakumbi luncedo kwinqanaba le-ferritin, elilinganisa ukugcinwa kwesinyithi emzimbeni wakho. Iqondo eliphantsi le-ferritin lihambelana nokusilela kwesinyithi.

Ukwahlula Ukunqongophala kwe-Iron Anemia Ukususela kwiThalassemia Trait

Ukwahlula kokuqala kukubalwa kweeseli zegazi (kubhalwe ngeRBC).

Ngokonakala kwintsimbi, eli xabiso liphantsi ngoba umongo wethambo awukwazi ukuvelisa iiseli ezibomvu zegazi. Kwi-thalassemia, uRBC iqhelekile ukuphakanyiswa. Inqanaba eliqhelekileyo le-ferritin lingakwazi ukulawula ukungabikho kwensimbi.

Uvavanyo oluthe ngqo, ngamanye amaxesha lubizwa ngokuthi i-hemoglobin electrophoresis okanye uhlolo lwe-hemoglobinopathy, lusetyenziswa iintlobo ezahlukeneyo ze-hemoglobin egazini lethu. Kumntu omdala, kufuneka kube ne-hemoglobin A ne-A2. Abantu abanomzila we-beta thalassemia baya kuphakama kwi-hemoglobin A2 kunye / okanye kwi-F (fetal). Akukho luvavanyo olulula lwe-alpha thalassemia. Ngokuqhelekileyo, ugqirha ulawula ukungabikho kwesinyithi kunye ne-beta thalassemia.

Xa izi zifo zimbini zilawulwa ngaphandle, i-alpha thalassemia trait is diagnostic diagnostic.

Ngoko Ungayithuthukisa njani i-Anemia yakho?

Unyango alufunanga okanye alucebisi. Le meko yomphefumlo wonke kunye ne-anemia elula kunye neeseli zegazi ezibomvu. Abantu abanempawu ze-thalassemia akufanele bathathe ukuxhaswa kwesebe njengoko oku kungayi kuphucula i-anemia yakho. Ukuba nomgangatho we-thalassemia akufanele kukubangela nayiphi na imicimbi yezempilo.

Kutheni Kubalulekile Ukukwazi Ukuba Unayo iThalassemia Trait

Ukuba wena kunye nomlingani wakho unomxholo ofanayo we-thalassemia (zombini i-alpha okanye zombini i-beta), unalo-1 kwi-4 (25%) wokuba nomntwana onesifo se-thalassemia Isifo se-Thalassemia sinokusukela kwi-anemia esilinganiselweyo ukuya kwi-anemia esingafunekiyo efuna igazi leenyanga ku gxothwa.