Motherhood In-Style Magazine

Family. Parenting. Building Homes.

Sickle Cell Disease: Expert, Dr. Taiwo Aderemi Stresses On Early Genotype Testing As Preventive Strategy

Sickle Cell Disease (SCD) is a group of blood disorders typically inherited from the parents. The Sickle Cell Hope Alive Foundation (SCHAF) has said that early genotype testing and screening remains the key preventive strategy against the disease.

SCHAF Medical Advisor, Dr. Taiwo Aderemi, made this known during a sensitisation and awareness exercise on SCD at Agbeni Market, in the Ibadan metropolis on Thursday, News Agency of Nigeria (NAN) reports.

Aderemi, a family health physician, said that sickle cell remained endemic in the country due to ignorance on the importance of genotype testing and premarital counseling. The physician said:

“Nigeria remains the country with the highest prevalence rate of SCD in the world. The disease continues to be endemic in the country because of lack of adequate awareness, and many couples with wrong matching of conflicting genotypes are still marrying one another.

READ ALSO: Wale Fanu, 68, Schools Us on How to Manage Sickle Cell Disease After Doctor Told His Mum That He Might Not Live Past 21

Premarital genotype screening presents an opportunity for intending couples to become informed about their genetic predisposition to diseases and for couples to be aware of the possible genetic characteristics of their children.

It is important that we continue to raise awareness on the importance of genotype testing, especially given the high rate of sickle cell in the country.”

According to him, reducing the prevalence of sickle cell disease is important because of the burden it constitutes not only to the country but also to families. The medical practitioner added:

READ ALSO: A Spotlight on How Ignorance Runs Deep in Africa as Children Living With Sickle Cell Disease Are Killed By their Parents

“Problems in sickle cell disease begin around 5 to 6 months of age. A number of health problems may develop, such as bone pain, anaemia, swelling in the hands and feet, end organ damage, leg ulcer, bacterial infections, and stroke.

“All these problems are consistent characteristics of SCD and they pose significant financial and psychological problem to the sufferer and the family. Therefore, scaling up awareness and acceptance of genetic screening is crucial to reducing its public health burden.”

Leave A Comment

Your email address will not be published.