‘Wrong genotype diagnosis contributes to high rate of SCD in Nigeria’

‘Wrong genotype diagnosis contributes to high rate of SCD in Nigeria’

by Joseph Anthony
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The Sickle Cell Hope Alive Foundation (SCHAF) has said wrong genotype diagnosis is a major contributor to the high prevalence of Sickle Cell Disease (SCD) in Nigeria.

Its President, Prof. Adeyinka Falusi, stated this on Monday at a media briefing in Ibadan, the Oyo State capital.

The News Agency of Nigeria (NAN) reports that the news conference was held to kick start the annual “Know Your Genotype (KYG) Workshop” organised by the NGO for school-age children and parents.

The workshop had the tagline: “Changing the Dynamics to Reduce the Burden of SCD in Nigeria.”

Falusi, a Professor of Haematology and Genetics, said the most commonly used diagnostic tests for genotype was costly and might take weeks, which could result in misdiagnosis.

“SCD is the commonest genetic inherited blood disorder in Nigeria affecting over four million individuals and with about 40 million sickle cell trait carriers.

“In Nigeria, genotype testing is very difficult and sometimes inaccurate; we cannot talk about awareness of SCD without accessible and affordable genotype testing methods.

“Genotype wrong diagnosis has resulted in people choosing incompatible partners and spouses, thus resulting in more children being born with SCD.”

“SCHAF is stepping in to support the government to fashion out ways in which we can reduce the public health burden of SCD through accurate diagnosis and awareness, which are hallmarks of prevention strategy,” she said.

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