Read Fast Facts for Patients: Alpha Thalassemia [Arabic]

Fast Facts for Patients: Alpha Thalassemia [Arabic]

Kevin H. M. Kuo

4.9/5 (33329 ratings)

Description:This booklet helps you understand alpha thalassemia (AT) so that you can talk to your medical team about your condition and its treatment. AT is a blood condition you are born with. You have to inherit a gene change from both parents to have AT. If you inherit a gene change from one parent, you are a carrier but don’t have the condition. If your partner is also a carrier, you have a chance of having a child with AT. AT is most common in people with ancestry from Southeast and South Asia, Africa, the Middle East and around the Mediterranean. There are two pairs of genes involved in AT – you may have one, two, three or four gene changes. There are also different types of gene changes – the gene can either be missing or damaged. How severe your AT is depends on the number and type of gene changes you have. AT major (four gene changes) is typically fatal before or shortly after birth without intervention. It remains a lifelong condition but can now be managed with treatment.We have made it easy for you to find a PDF Ebooks without any digging. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Fast Facts for Patients: Alpha Thalassemia [Arabic]. To get started finding Fast Facts for Patients: Alpha Thalassemia [Arabic], you are right to find our website which has a comprehensive collection of manuals listed.
Our library is the biggest of these that have literally hundreds of thousands of different products represented.

Pages: 50

Format: PDF, EPUB & Kindle Edition

Publisher: Karger Medical and Scientific Publishers

Release: 2025

ISBN: Gz6hEQAAQBAJ

Description: This booklet helps you understand alpha thalassemia (AT) so that you can talk to your medical team about your condition and its treatment. AT is a blood condition you are born with. You have to inherit a gene change from both parents to have AT. If you inherit a gene change from one parent, you are a carrier but don’t have the condition. If your partner is also a carrier, you have a chance of having a child with AT. AT is most common in people with ancestry from Southeast and South Asia, Africa, the Middle East and around the Mediterranean. There are two pairs of genes involved in AT – you may have one, two, three or four gene changes. There are also different types of gene changes – the gene can either be missing or damaged. How severe your AT is depends on the number and type of gene changes you have. AT major (four gene changes) is typically fatal before or shortly after birth without intervention. It remains a lifelong condition but can now be managed with treatment.We have made it easy for you to find a PDF Ebooks without any digging. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Fast Facts for Patients: Alpha Thalassemia [Arabic]. To get started finding Fast Facts for Patients: Alpha Thalassemia [Arabic], you are right to find our website which has a comprehensive collection of manuals listed.
Our library is the biggest of these that have literally hundreds of thousands of different products represented.

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Fast Facts for Patients: Alpha Thalassemia [Arabic]

Fast Facts for Patients: Alpha Thalassemia [Arabic]

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