[Congenital methaemoglobinaemia--a rare cause of dyspnoea and cyanosis]

Ugeskr Laeger. 2011 Aug 29;173(35):2133-4.
[Article in Danish]

Abstract

Dyspnoea in young people often leads to the diagnosis of asthma. A young female (with related parents) showed symptoms of cyanosis, dyspnoea and fatigue during physical activity despite asthma medication. High levels of methaemoglobin were measured. Genetic testing showed homozygote type 1b5r-deficiency. Cyanosis and lacking effect of asthma treatment should lead to further diagnostic evaluation with arterial blood gas analyses, including assessment of methaemoglobin. Congenitally inherited methaemoglobinaemia is a rare disease, but its diagnosis is important to ensure correct handling and treatment.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Asthma / diagnosis
  • Cyanosis / etiology*
  • Cytochrome-B(5) Reductase / genetics
  • Diagnosis, Differential
  • Dyspnea / etiology*
  • Female
  • Homozygote
  • Humans
  • Methemoglobinemia / complications
  • Methemoglobinemia / congenital*
  • Methemoglobinemia / diagnosis
  • Methemoglobinemia / genetics
  • Young Adult

Substances

  • Cytochrome-B(5) Reductase