Congenital Methemoglobinemia is a rare condition that may mimic congenital heart diseases. There are two types of congenital Methemoglobinemia. The type I is usually benign. The enzyme deficiency is limited to red blood cells. Clinically, the patient presents cyanosis without neurological disorders. Whereas, in type II, cyanosis is associated with severe neurological impairment.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271248 | PMC |
http://dx.doi.org/10.1002/ccr3.4422 | DOI Listing |
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