This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Classification by molecular genetics or genotype

Authoring team

99% of beta-thalassaemia genes have been characterised at the DNA level in terms of DNA deletions or point mutations. These DNA changes result in defects in transcription control, RNA processing and translation.

The beta-thalassaemias can be classified as beta0 or beta+. In beta0 thalassaemia no normal beta-chains are produced whilst in beta+ thalassaemia beta-chain production is impaired.

Since alpha-chain production is normal there is an excess of alpha-chains. These alpha-chains combine with available delta- and gamma-chains resulting in increased levels of Hb-A2 and Hb-F respectively.

The nature and severity of symptoms is dependent upon the level of beta-globin production and the amount of Hb-A2 and Hb-F present. This is in part dependent upon whether the individual is homozygous or heterozygous for a beta0 or beta+ allele.


Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.