Methemoglobinemia in an elderly patient with glucose-6-phosphate dehydrogenase deficiency: A case report

Kowthar S. Hassan; Arwa Z. Al-Riyami; Mohamed Al-Huneini; Khalil Al-Farsi; Murtadha Al-Khabori

doi:10.5001/omj.2014.33

Methemoglobinemia in an elderly patient with glucose-6-phosphate dehydrogenase deficiency: A case report

Kowthar S. Hassan, Arwa Z. Al-Riyami, Mohamed Al-Huneini, Khalil Al-Farsi, Murtadha Al-Khabori^*

^*المؤلف المقابل لهذا العمل

Haematology

نتاج البحث: المساهمة في مجلة › Article › مراجعة النظراء

10 اقتباسات (Scopus)

ملخص

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by low levels of the G6PD enzyme. It is present worldwide but with more prevalence in the Middle East and the Mediterranean areas. We report a case of severe hemolysis due to G6PD deficiency manifesting as methemoglobinemia in a 70 year old Omani male never known to have any previous hemolytic episodes or previously diagnosed of G6PD deficiency.

اللغة الأصلية	English
الصفحات (من إلى)	135-137
عدد الصفحات	3
دورية	Oman Medical Journal
مستوى الصوت	29
رقم الإصدار	2
المعرِّفات الرقمية للأشياء	https://doi.org/10.5001/omj.2014.33
حالة النشر	Published - 2014

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???subjectarea.asjc.2700.2700???

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10.5001/omj.2014.33

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abstract = "Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by low levels of the G6PD enzyme. It is present worldwide but with more prevalence in the Middle East and the Mediterranean areas. We report a case of severe hemolysis due to G6PD deficiency manifesting as methemoglobinemia in a 70 year old Omani male never known to have any previous hemolytic episodes or previously diagnosed of G6PD deficiency.",

keywords = "G6PD deficiency, Hemolysis, Methemoglobinemia",

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T1 - Methemoglobinemia in an elderly patient with glucose-6-phosphate dehydrogenase deficiency

T2 - A case report

AU - Hassan, Kowthar S.

AU - Al-Riyami, Arwa Z.

AU - Al-Huneini, Mohamed

AU - Al-Farsi, Khalil

AU - Al-Khabori, Murtadha

PY - 2014

Y1 - 2014

N2 - Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by low levels of the G6PD enzyme. It is present worldwide but with more prevalence in the Middle East and the Mediterranean areas. We report a case of severe hemolysis due to G6PD deficiency manifesting as methemoglobinemia in a 70 year old Omani male never known to have any previous hemolytic episodes or previously diagnosed of G6PD deficiency.

AB - Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder characterized by low levels of the G6PD enzyme. It is present worldwide but with more prevalence in the Middle East and the Mediterranean areas. We report a case of severe hemolysis due to G6PD deficiency manifesting as methemoglobinemia in a 70 year old Omani male never known to have any previous hemolytic episodes or previously diagnosed of G6PD deficiency.

KW - G6PD deficiency

KW - Hemolysis

KW - Methemoglobinemia

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DO - 10.5001/omj.2014.33

M3 - Article

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AN - SCOPUS:84897148447

SN - 1999-768X

VL - 29

SP - 135

EP - 137

JO - Oman Medical Journal

JF - Oman Medical Journal

IS - 2

ER -

Methemoglobinemia in an elderly patient with glucose-6-phosphate dehydrogenase deficiency: A case report

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