thalassemias

[US]/ˌθæləˈsiːmiəz/
[UK]/ˌθələˈsiːmiəz/

Translation

n. Arvede blodsygdomme, der er karakteriseret ved defekt hemoglobinsyntese.

Phrases & Collocations

thalassemias are

talassemier er

thalassemias include

talassemier omfatter

thalassemias cause

talassemier forårsager

in thalassemias

i talassemier

different thalassemias

forskellige talassemier

thalassemias result

talassemier resulterer

treating thalassemias

at behandle talassemier

managing thalassemias

at håndtere talassemier

thalassemias affect

talassemier påvirker

thalassemias involve

talassemier involverer

Example Sentences

thalassemias are inherited blood disorders characterized by abnormal hemoglobin production.

Thalassemier er arvelige blodsygdomme, der er karakteriseret ved abnorm produktion af hemoglobin.

thalassemias affect millions of people worldwide, particularly in mediterranean and asian populations.

Thalassemier påvirker millioner af mennesker verden over, især i mediterrene og asiatiske populationer.

thalassemias range from mild to severe forms, with varying clinical presentations.

Thalassemier varierer fra lette til alvorlige former med forskellige kliniske præsentationer.

thalassemias require lifelong management and regular monitoring by healthcare professionals.

Thalassemier kræver livslang behandling og regelmæssig overvågning af sundhedsprofessionelle.

thalassemias result in chronic anemia that can significantly impact quality of life.

Thalassemier fører til kronisk anæmi, som kan have betydelig indflydelse på livskvaliteten.

thalassemias are classified into alpha and beta types based on the affected globin chains.

Thalassemier klassificeres i alfa- og beta-typer baseret på de påvirkede globin-kæder.

thalassemias can be diagnosed through comprehensive blood tests and genetic analysis.

Thalassemier kan diagnosticeres gennem omfattende blodprøver og genetisk analyse.

thalassemias occur more frequently in regions where malaria has been endemic.

Thalassemier optræder hyppigere i områder, hvor malarie har været endemisk.

thalassemias involve mutations in genes that regulate hemoglobin synthesis.

Thalassemier involverer mutationer i gener, der regulerer hemoglobinsyntese.

thalassemias vary in severity from asymptomatic carriers to life-threatening conditions.

Thalassemier varierer i alværdsgrad fra asymptomatiske bærere til livstruende tilstande.

thalassemias often require regular blood transfusions to maintain adequate hemoglobin levels.

Thalassemier kræver ofte regelmæssige blodtransfusioner for at opretholde tilstrækkelige hemoglobin niveauer.

thalassemias pose significant challenges for genetic counseling and family planning.

Thalassemier stiller betydelige udfordringer for genetisk rådgivning og familieplanlægning.

thalassemias can lead to iron overload as a complication of repeated transfusions.

Thalassemier kan føre til jernoverbelastning som en komplikation ved gentagne transfusioner.

thalassemias are more prevalent in certain ethnic groups due to evolutionary selection pressure.

Thalassemier er mere udbredt i bestemte etniske grupper på grund af evolutionær selektionstryk.

thalassemias involve complex treatment protocols including iron chelation therapy.

Thalassemier involverer komplekse behandlingsprotokoller, herunder jernchelationstherapi.

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