thalassemia major Meaning in Bengali
Noun:
থ্যালাসেমিয়া প্রধান,
Similer Words:
thalassemiasthank offering
thank you
thanks to
thanksgiving cactus
thankworthy
that is to say
that is why
that much
that place
that'd
that's
thatch tree
thatched cottage
thaught
thalassemia major's Usage Examples:
thalassemia major which vary from asymptomatic or mild symptoms to severe anemia requiring lifelong transfusions.
Individuals with beta thalassemia major.
The situation of both alleles determines the clinical picture: β thalassemia major (Mediterranean anemia or Cooley anemia) is caused by a βo/βo genotype.
Kreger et al combining a retrospective review of three cases of alpha thalassemia major and a literature review of 17 cases found that in utero transfusion.
attributed to various anemias, most often; beta thalassemia major, a form of microcytic anemia.
In β thalassemia major the beta hemoglobin chain is completely.
Homozygous Hb Lepore is similar to beta-thalassemia major; however, the clinical course is variable.
Severely anemic fetuses, including those with Rh disease and alpha thalassemia major, can be treated with blood transfusions while still in the womb.
than deferoxamine in treating myocardial siderosis in patients with thalassemia major: DFP is thought to improve the function of mitochondria in the heart.
inherited genetic mutation in one (Beta thalassemia minor) or both (Beta thalassemia major) of the Beta globin alleles on chromosome 11.
RDW is seen in iron deficiency anemia and decreased or normal in thalassemia major (Cooley's anemia), thalassemia intermedia Anisocytosis with normal.
deferoxamine may increase the risk of hearing loss in patients with thalassemia major.
of iron chelation therapy with oral deferiprone in patients with thalassemia major".
deficiency) Hematologic diseases Hemoglobinopathies Sickle cell disease β thalassemia major (Cooley's anemia) Anemias Aplastic anemia Diamond–Blackfan anemia.
variability in the therapeutic response to deferiprone in patients with thalassemia major".
18-year-old male patient in France with beta-thalassemia major had been successfully treated.
Beta-thalassemia major is an inherited blood disease in which.
Patients with beta thalassemia major are more affected and are recommended to receive transfusion throughout.
"Prevalence and severity of liver disease in patients with b thalassemia major.
lymphoma), and severe anaemia (such as myelodysplastic syndrome, thalassemia major and severe aplastic anaemia).
Synonyms:
thalassaemia major; Cooley's anemia; thalassaemia; Mediterranean anemia; Mediterranean anaemia; Cooley's anaemia; thalassemia;
Antonyms:
offence; offense; defence; defense;