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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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hacettepe University Institute of Child Health
2009-04-01
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| Edice: | The Turkish Journal of Pediatrics |
| On-line přístup: | https://turkjpediatr.org/article/view/2285 |
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