hemolysis induced by glucose-6-phosphate dehydrogenase deficiency and its association with sex in children

Authors

esmaeel sadeghi department of pediatrics, namazee hospital, shiraz, iran.

perikala vijayananda kumar

mansour haghshenas

hamed jalaeian

abstract

background: glucose-6-phosphate dehydrogenase (g6pd) deficiency is the most common enzyme disorder in human. the aim of this study was to determine the prevalence of g6pd deficiency among children and evaluate its association with abo/rh blood groups.   method: blood samples of 3401 asymptomatic children were analyzed and compared with 317 children who were admitted to hospital because of hemolysis resulted from g6pd deficiency.   results: among asymptomatic children 375 (11%) were g6pd deficient. male to female ratio for this group was 4.2:1 and for the hemolytic group was 2.5:1 (p=0.004). two hundred and sixty-seven (84.2%) of the patients with hemolysis were younger than 2 years, with the peak age of hemolysis between 2 and 3 years (27.7%). the overall rate of hemolysis caused by g6pd deficiency was 12.3% during the 3 consecutive months of fresh fava bean consumption. blood groups o + , a + , and b + together constituted 87.1%, 87.7%, and 84% of the blood groups among normal children, asymptomatic g6pd deficient subjects, and those with g6pd deficiency related hemolysis respectively (p=0.367). seven percent of the normal children and asymptomatic g6pd deficient subjects were rh - vs 9.7 % of g6pd deficient children with hemolysis (p=0.16).   conclusion: the prevalence of g6pd deficiency among the children was 11%. male to female ratio was greater in non- hemolytic vs hemolytic group so that the female share was higher in hemolytic group than in the other two groups (p=0.004). the distribution of abo blood groups was similar among asymptomatic non-g6pd deficient, asymptomatic g6pd-deficient, and g6pd-deficient children with hemolysis. the distribution of rh - types among the g6pd-deficient children with hemolysis and the other two groups was similar (9.7% vs 7%, p=0.16).

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Hemolysis Induced by Glucose-6-Phosphate Dehydrogenase Deficiency and Its Association with Sex in Children

Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder in human. The aim of this study was to determine the prevalence of G6PD deficiency among children and evaluate its association with ABO/Rh blood groups. Method: Blood samples of 3401 asymptomatic children were analyzed and compared with 317 children who were admitted to hospital because of hemolys...

full text

Intravascular Hemolysis Due to Glucose‐6‐Phosphate Dehydrogenase Deficiency in a Patient with Aluminium Phosphide Poisoning

Aluminium Phosphide poisoning and glucose‐6‐phosphate dehydrogenase deficiency are two commonly seen clinical presentations in Iran. However, hemolysis associated with Aluminium Phosphide poisoning is very rare. We report a case of concurrent Aluminium Phosphide poisoning and glucose‐6‐phosphate dehydrogenase deficiency in a 24 year old man presenting with intravascular hemolysis. Key words...

full text

Clinical Manifestations of Acute Hemolysis in Children with Glucose-6-Phosphate Dehydrogenase Deficiency in Fars Province, Iran

Background: Absence or deficiency in Glucose-6-phosphate dehydrogenase (G6PD) enzyme in patients with G6PD deficiency presents with a wide spectrum of symptoms. This study evaluates the clinical features of acute hemolysis in children with G6PD deficiency. Materials and Methods: Seventy G6PD deficient children younger than 18 years old were included in this cross sectional study in Dastgheib H...

full text

Seizure following acute hemolysis caused by Glucose-6-phosphate dehydrogenase Deficiency

Background: Storage of platelet concentrates (PCs) at room temperature (20-24°C) limits its storage time to 5 Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited enzyme deficiency of the human red blood cells . Most of G6PD deficient individuals are asymptomatic, but acute hemolytic anemia may be presented with nausea, vomiting, abdominal pain, headache,...

full text

Fulminant hemolysis in glucose‐6‐phosphate dehydrogenase deficiency

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked disorder affecting some 400 million people worldwide. Though clinically silent, it may result in hemolysis on oxidative stress induced by drugs or infections. Viral hepatitis A with coexisting G6PD deficiency can be devastating associated with severe hemolysis, anemia, renal failure, and hepatic encephalopathy.

full text

Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia

Background: Jaundice is affecting over 60-80 percent of neonates in the first week of life. Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which is an important cause of pathologic hyperbilirubinemia, can lead to hemolytic anemia, jaundice and kernicterus. The present study was performed to determine the prevalence of G6PD deficiency among icteric neonates in Shirvan, Iran. Methods: This...

full text

My Resources

Save resource for easier access later


Journal title:
iranian journal of medical sciences

جلد ۳۵، شماره ۱، صفحات ۴۸-۰

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023