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Title: Frequency of haemoglobinopathies: a single-centre, cross-sectional study from Islamabad, Pakistan
Authors: Waheed, U.
Satti, H.S.
Farooq, N.
Zaheer, H.A.
Issue Date: 2012
Language: English
Abstract: Thalassaemia is the most frequent hereditary disorder in Pakistan, with an estimated 8-10 million carriers. This single-centre study reported the frequency of haemoglobinopathies among 504 consecutive cases visiting Islamabad Diagnostic Centre for haemoglobin electrophoresis from July 2010 to February 2011. Haemoglobin electrophoresis was performed on cellulose acetate membrane, followed by staining and densitometric scanning of bands. A total of 143 [28.4%] subjects had haemoglobinopathies. The most predominant was thalassaemia trait [25.6%], followed by thalassaemia major [1.4%] and HbS or HbD [1.4%]. The gene frequencies for thalassaemia trait and major were 0.256 and 0.0139 respectively. The study provides support for continuing efforts towards early detection and characterization of haemoglobinopathies to control the affected births in Pakistan
Description: 1257-1259
Keywords: beta-Thalassemia
Hemoglobin, Sickle
Cross-Sectional Studies
Electrophoresis
Genotype
Subject: Hemoglobinopathies
URI: http://www.who.int/iris/handle/10665/118479
ISSN: 1020-3397
Other Identifiers: http://applications.emro.who.int/emhj/v18/12/EMHJ_2012_18_12_1257_1259.pdf
Appears in Collections:EMRO Journal Articles (EMHJ)



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