thalassaemia major

/ˌθæləˈsiːmiə ˈmeɪdʒər/

Tradução: Forma grave e hereditária da talassemia, causada pela redução ou ausência da produção de cadeias de globina, levando a anemia severa que exige transfusões sanguíneas regulares e acompanhamento médico.

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phrase

/ˌθæləˈsiːmiə ˈmeɪdʒər/C1formalmedical

Тяжелое наследственное заболевание крови, характеризующееся снижением выработки гемоглобина, приводящее к анемии, требующее регулярных переливаний крови и медицинского наблюдения.
Enfermedad hereditaria grave de la sangre caracterizada por una producción reducida de hemoglobina, que provoca anemia y requiere transfusiones de sangre regulares y supervisión médica.
Forme grave de thalassémie, maladie héréditaire du sang caractérisée par une production insuffisante d'hémoglobine, entraînant une anémie sévère nécessitant des transfusions sanguines régulières et un suivi médical.
Schwere erbliche Blutkrankheit, bei der zu wenig Hämoglobin gebildet wird, was zu einer Anämie führt und regelmäßige Bluttransfusionen sowie medizinische Betreuung erfordert.
Forma grave e hereditária da talassemia, causada pela redução ou ausência da produção de cadeias de globina, levando a anemia severa que exige transfusões sanguíneas regulares e acompanhamento médico.
重型地中海贫血，是一种严重的遗传性血液病，因血红蛋白合成减少导致贫血，需要定期输血和医疗监护。
مرض وراثي شديد في الدم يتميز بانخفاض إنتاج الهيموغلوبين مما يؤدي إلى فقر دم يحتاج إلى نقل دم منتظم ومتابعة طبية.

A severe inherited blood disorder characterized by reduced production of hemoglobin, leading to anemia, requiring regular blood transfusions and medical management.

Severe inherited blood disorderC2formal
A serious genetic blood disorder characterized by reduced production of hemoglobin, leading to severe anemia and requiring regular blood transfusions.
Talassemia maior
- Patients with thalassaemia major require lifelong blood transfusions.
- Thalassaemia major is typically diagnosed in early childhood.
- Treatment for thalassaemia major includes iron chelation therapy to prevent organ damage.