Methemoglobinemia classification: Difference between revisions
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==Classification== | ==Classification== | ||
'''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 | |||
==References== | ==References== |
Revision as of 01:27, 22 April 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Classification
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