Journal of Applied Hematology

CASE REPORT
Year
: 2016  |  Volume : 7  |  Issue : 3  |  Page : 108--110

Hereditary methemoglobinemia manifesting in adolescence


Mazen A Badawi1, Maha A Badawi2, Siraj O Wali1, Rajaa Z Alsaggaf3 
1 Department of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
2 Department of Hematology, King Abdulaziz University, Jeddah, Saudi Arabia
3 Department of Medicine, King Abdullah Medical City, Makkah, Saudi Arabia

Correspondence Address:
Maha A Badawi
Department of Hematology, Faculty of Medicine, King Abdulaziz University, P.O. Box 80215, Jeddah 21589
Saudi Arabia

Methemoglobinemia is an uncommon cause of cyanosis that may present at any age. Although acquired methemoglobinemia secondary to exposure to oxidative stressors is the most common cause of methemoglobinemia in adults, hereditary methemoglobinemia has to be considered in patients presenting with cyanosis during infancy and childhood. We report the case of a patient who was investigated for cyanosis that was only noted at the age of 15 years. Despite the negative family history, he was diagnosed with hereditary autosomal recessive methemoglobinemia with no other factors that can be identified to cause such an elevation of methemoglobin level. This case illustrates that hereditary methemoglobinemia has to be considered in such patients even if they were completely asymptomatic for many years of their lives.


How to cite this article:
Badawi MA, Badawi MA, Wali SO, Alsaggaf RZ. Hereditary methemoglobinemia manifesting in adolescence.J Appl Hematol 2016;7:108-110


How to cite this URL:
Badawi MA, Badawi MA, Wali SO, Alsaggaf RZ. Hereditary methemoglobinemia manifesting in adolescence. J Appl Hematol [serial online] 2016 [cited 2022 Dec 2 ];7:108-110
Available from: https://www.jahjournal.org/article.asp?issn=1658-5127;year=2016;volume=7;issue=3;spage=108;epage=110;aulast=Badawi;type=0