| Plural | thalassemias |
thalassemia major
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thalassemia minor
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thalassemia trait
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alpha thalassemia
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beta thalassemia
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thalassemia screening
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thalassemia test
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thalassemia carrier
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thalassemia diagnosis
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thalassemia patient
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thalassemia is a hereditary blood disorder characterized by abnormal hemoglobin production.
Thalassemia er en arvelig blodsygdom, der er karakteriseret ved abnorm produktion af hemoglobin.
many people are unaware they carry the thalassemia gene until their child is diagnosed.
Mange mennesker ved ikke, at de bærer thalassemia-genen, før deres barn diagnosticeres.
regular blood transfusions are essential for patients with thalassemia major.
Regelmæssige blodtransfusioner er afgørende for patienter med thalassemia major.
prenatal screening can detect thalassemia in unborn babies with high accuracy.
Fødselsforberedende screening kan med stor præcision opdage thalassemia hos udfødt børn.
iron overload is a serious complication that requires chelation therapy in thalassemia patients.
Jernoverbelastning er en alvorlig komplikation, der kræver chelationstherapi hos thalassemia-patienter.
thalassemia carrier screening is recommended for couples planning to start a family.
Det anbefales, at par, der planlægger at have børn, gennemgår screening for at se, om de bærer thalassemia-genen.
the severity of thalassemia depends on how many mutated genes a person inherits.
Syvretiden af thalassemia afhænger af, hvor mange muterede gener en person arver.
advances in gene therapy offer new hope for curing thalassemia in the future.
Fremskridt inden for genetisk terapi giver nye muligheder for at helbrede thalassemia i fremtiden.
thalassemia intermedia patients experience moderate symptoms compared to the major form.
Patients med thalassemia intermedia oplever moderate symptomer i forhold til den alvorlige form.
children with thalassemia major often require lifelong medical care and support.
Børn med thalassemia major har ofte brug for livslang medicinsk pleje og støtte.
genetic counseling helps families understand the risks of passing thalassemia to their children.
Genetisk rådgivning hjælper familier med at forstå risikoen for at overføre thalassemia til deres børn.
thalassemia is most prevalent in mediterranean, african, and southeast asian populations.
Thalassemia er mest udbredt i mediterrene, afrikanske og sydøstasiatiske populationer.
thalassemia major
Danish_translation
thalassemia minor
Danish_translation
thalassemia trait
Danish_translation
alpha thalassemia
Danish_translation
beta thalassemia
Danish_translation
thalassemia screening
Danish_translation
thalassemia test
Danish_translation
thalassemia carrier
Danish_translation
thalassemia diagnosis
Danish_translation
thalassemia patient
Danish_translation
thalassemia is a hereditary blood disorder characterized by abnormal hemoglobin production.
Thalassemia er en arvelig blodsygdom, der er karakteriseret ved abnorm produktion af hemoglobin.
many people are unaware they carry the thalassemia gene until their child is diagnosed.
Mange mennesker ved ikke, at de bærer thalassemia-genen, før deres barn diagnosticeres.
regular blood transfusions are essential for patients with thalassemia major.
Regelmæssige blodtransfusioner er afgørende for patienter med thalassemia major.
prenatal screening can detect thalassemia in unborn babies with high accuracy.
Fødselsforberedende screening kan med stor præcision opdage thalassemia hos udfødt børn.
iron overload is a serious complication that requires chelation therapy in thalassemia patients.
Jernoverbelastning er en alvorlig komplikation, der kræver chelationstherapi hos thalassemia-patienter.
thalassemia carrier screening is recommended for couples planning to start a family.
Det anbefales, at par, der planlægger at have børn, gennemgår screening for at se, om de bærer thalassemia-genen.
the severity of thalassemia depends on how many mutated genes a person inherits.
Syvretiden af thalassemia afhænger af, hvor mange muterede gener en person arver.
advances in gene therapy offer new hope for curing thalassemia in the future.
Fremskridt inden for genetisk terapi giver nye muligheder for at helbrede thalassemia i fremtiden.
thalassemia intermedia patients experience moderate symptoms compared to the major form.
Patients med thalassemia intermedia oplever moderate symptomer i forhold til den alvorlige form.
children with thalassemia major often require lifelong medical care and support.
Børn med thalassemia major har ofte brug for livslang medicinsk pleje og støtte.
genetic counseling helps families understand the risks of passing thalassemia to their children.
Genetisk rådgivning hjælper familier med at forstå risikoen for at overføre thalassemia til deres børn.
thalassemia is most prevalent in mediterranean, african, and southeast asian populations.
Thalassemia er mest udbredt i mediterrene, afrikanske og sydøstasiatiske populationer.
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