Cututtuka na Sickle-Cell, Types, Dabbobi, da Jiyya

Sickle cell cell (SCD) wani nau'i ne na ainihi wanda aka gaji a inda yaduwar kwayoyin jini ta canza daga tsarin al'ada (kama da wani donut) a cikin siffar dogon lokaci kamar sickle ko banana. Wadannan kwayoyin jini masu launin jini suna da wahalar da ke gudana ta hanyar jini kuma zasu iya yin makale. Jikin jikin ya gane wadannan kwayoyin jini kamar yaduwa kuma ya halakar da su sauri fiye da yadda ya saba haifar da anemia.

Yaya Yaya Mai Samun SCD?

Ciwon sikila ne ya gaji, saboda haka an haifi mutum tare da shi. Don mutum ya gaji SCD, duka iyaye dole ne suna da sutura. A cikin sababbin siffofin SCD, iyaye ɗaya suna da ƙwayar cuta kuma ɗayan iyaye yana da alamar hawan haemoglobin C ko beta thalassemia trait. Lokacin da iyaye biyu suna da nau'in sutura (ko wani nau'i), suna da 1 cikin 4 na samun yarinya da SCD. Wannan hadarin yakan faru a kowace ciki.

Irin Sickle Cell Cell

Mafi yawan cututtukan cututtukan ciwon sikila ana kiranta homoglobin SS. Sauran manyan nau'ikan su ne: hemoglobin SC, sickle beta zero thalassemia, da kuma sickle beta tare da thalassemia. Hemoglobin SS da sickle beta zero thalassemia sune cututtukan cututtukan cututtukan ciwon sikila kuma wasu lokuta ana kiransa da cutar anadia. Ana dauke da cutar cututtukan Hemoglobin SC a matsayin matsakaici kuma a gaba ɗaya, sickle beta tare da lalatarmia shine mummunan yanayin ciwon sikila.

Ta Yaya Mutane Aka Bincike Da Ciwo na Sickle-Cell?

A Amurka, ana jarraba dukan jariri jarrabawar SCD ba da jimawa ba bayan haihuwar su a matsayin ɓangare na shirin gwajin yara . Idan sakamakon ya kasance tabbatacce ga SCD, an sanar da dan jariri na dan jarida ko cibiyar ciwon sikila na gida game da sakamakon haka ana iya ganin mai haƙuri a asibitin sikila.

A ƙasashe da ba su yi jarrabawar jariri ba, mutane sukan kamu da cutar SCD a matsayin yara lokacin da suka fara samun alamun bayyanar.

Kwayar cutar SCD

Saboda ciwon sikila (SCD) wani ɓarna ne daga cikin jinin jinin jiki duka za'a iya shafar jikin.

Jiyya na SCD