Recessive congenital methemoglobinemia in immediate generations

Recessive congenital methemoglobinemia in immediate generations

We report herein on our observation of recessive congenital methemoglobinemia(type I), an autosomal recessive disorder, in immediate generations (in amother and her daughter). Molecular analysis revealed a mechanism ofinheritance not reported previously, despite the high probability of occurrencein autosomal recessive disorders. This report is also the first publicationdescribing an extremely rare mutation (Arg50Gln) causing this disorder inthe Turkish population.

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  • 4. Percy MJ, McFerran NV, Lappin TR. Disorders of oxidised haemoglobin. Blood Rev 2005; 19: 61-68.
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  • 8. Percy MJ, Barnes C, Crighton G, Leventer RJ, Wynn R, Lappin TR. Methemoglobin reductase deficiency: novel mutation is associated with a disease phenotype of intermediate severity. J Pediatr Hematol Oncol 2012; 34: 457-460.
Turkish Journal of Pediatrics-Cover
  • ISSN: 0041-4301
  • Yayın Aralığı: 6
  • Başlangıç: 1958
  • Yayıncı: Hacettepe Üniversitesi Çocuk Sağlığı Enstitüsü Müdürlüğü
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