By Kevin H.M. Kuo
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.
Product Details
ASIN : B0CKMRXZCP
Publisher : S. Karger
Publication date : October 31, 2023
Language : English
ISBN-13 : 978-3318073447

National Emergency Medicine Board Review, 17th Edition (2015)
Comprehensive Review of Blood Banking 2015 (CME Videos)
Management and Administration of Laboratories 2015 (CME Videos)
Orthopaedic Surgery Board Review 2015 (CME Videos)
The Brigham Board Review in Pulmonary Medicine 2016 (CME Videos)
Thoracic Imaging 2016 (CME Videos)
2020 Scottsdale Headache Symposium (CME VIDEOS)
Paediatric Dentistry: Principles and Practice, 2nd Edition (PDF)
Head and Neck Cancer: An Evidence-Based Team Approach
Pediatric Body MRI 2015 (CME Videos)
National Diagnostic Imaging Symposium 2015 (CME Videos)
Comprehensive Review of Urology 2015 (CME Videos)
Lippincott's Concise Illustrated Anatomy: Volume 1: Back, Upper Limb and Lower Limb
Lippincott's Concise Illustrated Anatomy: Volume 2: Thorax, Abdomen & Pelvis 


Reviews
There are no reviews yet.