Thalassemia secondary prevention: Difference between revisions
Jump to navigation
Jump to search
m (Template) |
Shyam Patel (talk | contribs) |
||
| Line 7: | Line 7: | ||
==Secondary Prevention== | ==Secondary Prevention== | ||
Secondary prevention for thalassemia focuses on preventing the birth of infants who could be at risk for thalassemia. Secondary prevention focuses on genetic counseling of patients who are known carriers of alpha-globin or beta-globin chain mutations. Education programs have been instituted in a variety of countries to address secondary prevention. | |||
==References== | ==References== | ||
Revision as of 16:53, 21 November 2017
|
Thalassemia Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Thalassemia secondary prevention On the Web |
|
American Roentgen Ray Society Images of Thalassemia secondary prevention |
|
Risk calculators and risk factors for Thalassemia secondary prevention |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.
Overview
Secondary Prevention
Secondary prevention for thalassemia focuses on preventing the birth of infants who could be at risk for thalassemia. Secondary prevention focuses on genetic counseling of patients who are known carriers of alpha-globin or beta-globin chain mutations. Education programs have been instituted in a variety of countries to address secondary prevention.