Sideroblastic anemia other diagnostic studies: Difference between revisions
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* Serum lead levels, | * Serum lead levels, | ||
** It is increased in sideroblastic anemia secondry to lead toxicity. | ** It is increased in sideroblastic anemia secondry to lead toxicity. | ||
Genetic testing in congenital sideroblasticemias, genetic testing is the most definitive means of establishing the specific diagnosis and characterizing the mutation. Genetic testing is performed by DNA sequence analysis using leukocytes from peripheral blood | |||
* Genetic testing in congenital sideroblasticemias, | |||
* genetic testing is the most definitive means of establishing the specific diagnosis and characterizing the mutation. Genetic testing is performed by DNA sequence analysis using leukocytes from peripheral blood | |||
==References== | ==References== | ||
Revision as of 19:13, 8 August 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:
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Overview
Other Diagnostic Studies
Other diagnostic studies for sideroblastic anemia include:
- Urine porphyrin profile may demonstrates
- Erythropoietic porphyria
- Serum lead levels,
- It is increased in sideroblastic anemia secondry to lead toxicity.
- Genetic testing in congenital sideroblasticemias,
- genetic testing is the most definitive means of establishing the specific diagnosis and characterizing the mutation. Genetic testing is performed by DNA sequence analysis using leukocytes from peripheral blood