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Frequency and types of hemoglobinopathies in children with microcytic anemia
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Abstract
Objective: To study the frequency and types of haemoglobinopathies in children with microcytic anaemia.
Method: The prospective study was conducted at the Paediatric Out-patient Department of Shifa Falahi Community Health Centre, Islamabad, Pakistan, from July to December, 2018, and comprised patients aged from 3 months to 14 years who had haemoglobin <10mg/dl and mean corpuscular volume <70fL. Serum ferritin and haemoglobin electrophoresis were done to check for iron deficiency anemia and haemoglobinopathies. Data was analysed using SPSS 23.
Results: Of 175 subjects, 33(18.9%) had haemoglobinopathies and 142(81.1%) had iron deficiency anaemia. Thalassemia trait 18(10.3%) was the leading cause amongst haemoglobinopathies, followed by thalassemia major 8(4.6 %) and intermedia 5(2.9%). There were 2(1.1%) patients with haemoglobin D.
Conclusion: The prevalence of hemoglobinopathies was high. Identification of haemoglobinopathies is important for proper treatment, antenatal screening and future genetic counselling.
Key Words: Haemoglobinopathy, Iron deficiency anaemia, Microcytic, MCV, IDA.
Pakistan Medical Association
Title: Frequency and types of hemoglobinopathies in children with microcytic anemia
Description:
Abstract
Objective: To study the frequency and types of haemoglobinopathies in children with microcytic anaemia.
Method: The prospective study was conducted at the Paediatric Out-patient Department of Shifa Falahi Community Health Centre, Islamabad, Pakistan, from July to December, 2018, and comprised patients aged from 3 months to 14 years who had haemoglobin <10mg/dl and mean corpuscular volume <70fL.
Serum ferritin and haemoglobin electrophoresis were done to check for iron deficiency anemia and haemoglobinopathies.
Data was analysed using SPSS 23.
Results: Of 175 subjects, 33(18.
9%) had haemoglobinopathies and 142(81.
1%) had iron deficiency anaemia.
Thalassemia trait 18(10.
3%) was the leading cause amongst haemoglobinopathies, followed by thalassemia major 8(4.
6 %) and intermedia 5(2.
9%).
There were 2(1.
1%) patients with haemoglobin D.
Conclusion: The prevalence of hemoglobinopathies was high.
Identification of haemoglobinopathies is important for proper treatment, antenatal screening and future genetic counselling.
Key Words: Haemoglobinopathy, Iron deficiency anaemia, Microcytic, MCV, IDA.
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