A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II
Recessive congenital methemoglobinemia (RCM) is a very rare disorder caused by NADH- cytochrome b5 reductase (cytb5r) deficiency. It has been classified into four types. Type I presents with mild cyanosis due to a significant deficiency of cytb5r in erythrocytes only. In type II, the deficien...
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| Main Authors: | Deniz Yüksel, Nesrin Senbil, Deniz Yilmaz, Neşe Yarali, Y K Yavuz Gürer |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Hacettepe University Institute of Child Health
2009-04-01
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| Series: | The Turkish Journal of Pediatrics |
| Online Access: | https://turkjpediatr.org/article/view/2285 |
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