Methemoglobinemia laboratory findings: Difference between revisions
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==Overview== | ==Overview== | ||
'''Congenital (Hereditary) Methemoglobinemia''' | |||
There are three main congenital conditions that lead to methemoglobinemia: | |||
1. Cytochrome b5 reductase deficiency and pyruvate kinase deficiency | |||
2. G6PD deficiency | |||
3. Presence of abnormal hemoglobin. | |||
'''Acquired or Acute Methemoglobinemia''' | |||
Most common cause include different oxidant drugs, toxins or chemicals | |||
==Laboratory Findings== | ==Laboratory Findings== |
Revision as of 11:14, 29 April 2018
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Overview
Congenital (Hereditary) Methemoglobinemia
There are three main congenital conditions that lead to methemoglobinemia:
1. Cytochrome b5 reductase deficiency and pyruvate kinase deficiency
2. G6PD deficiency
3. Presence of abnormal hemoglobin.
Acquired or Acute Methemoglobinemia
Most common cause include different oxidant drugs, toxins or chemicals