| Literature DB >> 18343696 |
Elisa Fermo1, Paola Bianchi, Cristina Vercellati, Anna Paola Marcello, Massimo Garatti, Ornella Marangoni, Wilma Barcellini, Alberto Zanella.
Abstract
We report the clinical and molecular characteristics of 6 new patients with recessive hereditary methemoglobinemia due to cytochrome b5 reductase deficiency. One patient was affected by Type-II disease with cyanosis and severe progressive neurological dysfunction, whereas the others displayed the benign Type-I phenotype. Methemoglobin levels ranged from 12.1% to 26.2% and cytochrome b5 reductase activity from 0 to 10% of normal. Eight different mutations were detected among the twelve mutated alleles identified, one splicing mutation, two stop codon, and five missense. Two mutations c. 82 C>T(Gln27STOP) and c. 136 C>T(Arg45Trp) are new. Prenatal diagnosis was performed in the family with Type-II disease.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18343696 DOI: 10.1016/j.bcmd.2008.02.002
Source DB: PubMed Journal: Blood Cells Mol Dis ISSN: 1079-9796 Impact factor: 3.039