Recessive congenital methemoglobinemia: a systematic review of reported cases
Abstract Background Recessive congenital methemoglobinemia (RCM) is a rare autosomal recessive disorder characterized by a deficiency of NADH-cytochrome b5 reductase. Under normal conditions, cytochrome b5 reductase and NADH reductase maintain methemoglobin in the physiological range by keeping heme...
Furkejuvvon:
| Váldodahkkit: | , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
BMC
2026-02-01
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| Ráidu: | Orphanet Journal of Rare Diseases |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1186/s13023-026-04215-7 |
| Fáddágilkorat: |
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