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With reference to National Sickle Cell Anaemia Elimination Mission, consider the following statements
The mission aims to eliminate Sickle Cell Anaemia by 2047.
The mission will cover the entire population from 0 to 18 years.
Sickle cell disease is an inherited group of blood disorders that is genetic in nature.
Select the correct statement.
1&2 only
2&3 only
1&3 only
All of the above
Only statements 1&3 are correct.
National Sickle Cell Anaemia Elimination Mission
Recently Prime Minster Narendra Modi launched National Sickle Cell Anaemia Elimination Mission to eliminate it by 2047.
National Sickle Cell Anaemia Elimination Program was introduced in the Union Budget 2023.
Mission: To improve care of all Sickle Cell Disease patients for their better future and to lower the prevalence of the disease through multi-faced coordinated approach towards screening and awareness strategies
Objectives of the Mission
Provision of affordable and accessible care to all SCD patients,
To ensure quality of care for SCD patients and
To reduce the prevalence of SCD.
It focuses on eliminating sickle cell disease, particularly among tribal populations of the country.
It is part of the National Health Mission (NHM), aims to eliminate sickle cell genetic transmission by the year 2047.
Over a period of three years, spanning from 2023-24 to 2025-26, the program targets screening approximately 7 crore people aged 0-40 years in affected tribal areas.
It is implemented in 17 high-focus states across the country.
Platforms such as monthly Village Health Sanitation and Nutrition Committee (VHSNC) shall be leveraged to make awareness about the disease.
Sickle cell disease (SCD)
Red blood cells contain hemoglobin, a protein that carries oxygen.
Sickle cell disease (SCD) is a chronic single gene disorder causing a debilitating systemic syndrome characterized by Chronic anaemia, Acute painful episodes, Organ infarction and chronic organ damage and Significant reduction in life expectancy.
SCD is a genetic condition that is present at birth.
It is inherited when a child receives two genes—one from each parent—that code for abnormal hemoglobin.
Hence option 3rd is correct.
By: Shubham Tiwari ProfileResourcesReport error
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