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thalassaemia

/ ˌθæləˈsiːmɪə /

noun

  1. Also called: Cooley's anaemiaa hereditary disease, common in many parts of the world, resulting from defects in the synthesis of the red blood pigment haemoglobin

“Collins English Dictionary — Complete & Unabridged” 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012


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Word History and Origins

Origin of thalassaemia1

New Latin, from Greek thalassa sea + -aemia , from it being esp prevalent round the eastern Mediterranean Sea
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Example Sentences

Examples are provided to illustrate real-world usage of words in context. Any opinions expressed do not reflect the views of Dictionary.com.

Crucially, it is only the adult form of haemoglobin that is affected by beta thalassaemia.

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People with beta thalassaemia do not produce enough haemoglobin, which is used by red blood cells to carry oxygen around the body.

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The same genetic procedure has been performed on a total of 45 patients with either sickle cell disease or another blood disorder called beta thalassaemia, which is caused by malformed haemoglobin.

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Abhijit suffered from thalassaemia major, a disorder where his haemoglobin count was dangerously low and he required frequent blood transfusions.

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Dr Amit Raithatha, from London, suffers from thalassaemia, a rare blood disorder that means he produces very little haemoglobin, which is used by blood cells to carry oxygen around the body.

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Thalassathalassemia