Congenital Methemoglobinemia is a rare neurologic condition which can mimic other diseases such as epilepsy syndromes and leukodystrophies. The responsible gene, CYB5R3, is not typically included on commonly order neurologic and epilepsy panels. We recommend that laboratories include this gene on these tests which often precede larger-scale genetic studies.
Keywords: CYB5R3; Cyanosis; developmental delay; leukodystrophy; methemoglobin reductase; methemoglobinemia type II; microcephaly.