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An inherited form of anemia is known as sickle cell anemia. It is a condition in which adequate oxygen can not be performed throughout your body as enough healthy red blood cells are not there. In addition, you may experience symptoms such as frequent chest, arm and leg pain, fatigue and your hands and feet may swell. You can also suffer from jaundice. You should visit an expert if observing pale skin, abdominal swelling, fever and stroke symptoms – difficulty walking, vision problem and so on. Keep reading.
Now, a point-of-care device will help determine if it has a sickle cell gene. And this identification can be done simply in 10 minutes. The Sickle Cell Support Society of Nigeria has urged health facilities to adopt this new method of diagnosing SCD in newborns. As part of the workshop organized by the Center of Excellence for Research and Training on Sickle Cell Disease of Abuja University, Professor Adekunle Adekile, President of the Society, has stated that in advanced countries such as the United Kingdom, a newborn baby must undergo a sickle cell test because it helps them to give a baby complete care.
He also said explained, because of the early diagnosis, the prospects have changed in these counties. Before that, most children had lost their lives before the age of 5 years. Earlier, the diagnosis was very expensive, but there are now simple and cheap methods to diagnose it. Early diagnosis can help to take preventive measures so that children do not develop complications that can cost them their lives.
Prof. Obiageli Nnodu and Director of the Center of Excellence for Research and Training on Sickle Cell Disease who organized the program says that the workshop was a pilot study
Source of Image : Shutterstock
Posted: 27 July 2018 11:32 am | Updated: July 27, 2018 11:35 am
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