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2015-2016 Thalassemia Outreach Intern Team1 Sign up for our newsletter2 New multidisciplinary center for Alpha Thalassemia Major4 Twin girls from China reunited at our thalassemia center5 Slides: Seattle thalassemia patient and family conference6 My Experience iwth Gene Therapy7 How you can help8 Visit our Facebook page9 Focus on Alpha Thalassemia, by Ash Lal MD10 Painted Turtle Camp July 17-2211 Thalassemia Fact Sheet12 Thalassemia: The Passion to Help Others13 14 Thank you, Italian Catholic Federation (ICF)!14 15 slideshow jquery by WOWSlider.com v8.2

The Demographics of Thalassemia

Demographics of Thalassemia
▶ Prevalence & Demographics: Worldwide

Thalassemia in California: The PHRESH Project

 
 
PHRESH fact sheet on thalassemia:
fact sheet
 

Prevalence and Demographics: Worldwide

children Thalassemia occurs across the globe, but is most prevalent among the following populations:

There are two main types of thalassemia trait: alpha thalassemia trait and beta thalassemia trait. Individuals who have beta thalassemia trait have one normal beta globin gene and one that is altered such that it makes little or no beta globin. There are subtypes of alpha thalassemia trait. Individuals with 'silent alpha thalassemia trait' are missing one alpha globin gene. When two alpha globin genes are missing, an individual is said to have 'alpha thalassemia trait'. This can occur in two different ways. The 'cis' type of alpha thalassemia trait occurs when the two genes are missing from the same chromosome. This type is most common in those of Southeast Asian, Chinese, or Mediterranean ancestry. The 'trans' type of alpha thalassemia trait occurs when the two genes are missing from different chromosomes. This type is most common in African Americans.

Thalassemia trait is generally not thought to cause health problems, although women with the trait may be more likely to develop anemia of pregnancy than women without the trait. Obstetricians sometimes treat this with folate supplementation. Most types of thalassemia traits cause the red blood cells to be smaller in size than usual, a condition called microcytosis. Sometimes this is inaccurately referred to as 'low blood'. Since iron deficiency is the most common cause of microcytosis, doctors sometimes mistakenly prescribe iron supplementation to individuals with thalassemia trait. Therefore, before prescribing iron supplements, doctors should rule out thalassemia trait and/or perform lab tests to evaluate iron levels. A person with thalassemia trait can also be iron deficient, but if he or she is not, iron supplements may result in excess body iron. Excessive iron can deposit in many areas of the body, causing organ damage in the long-term.

Updated 1/21/2015


Northern California Comprehensive Thalassemia Center
UCSF Benioff Children's Hospital Oakland
747 52nd Street, Oakland CA 94609   •   Phone: (510) 428-3651   •   Fax: (510) 450-5647
© 2003-2012 Children's Hospital & Research Center Oakland
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