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Ganes for Children Disabilities: Janajat disorder is found in some children. In this, the intellectual development of children is blocked. Now scientists have found the reason behind this.
Open way to treat brain.
Ganes for Children Disabilities: You must have noticed that some children have congenital intellectual deformity. Many diseases of the brain are responsible for this. Some children have a disease named Microcephone before and after birth, due to which the size of the head becomes small. At the same time some children suffer from Pontocerebeller hypoplasia-pontocerebellar hypoplasia disease. In this, brain stam and cerebellum are not developed, due to which the intellectual development of the child stops. Everything is fine in many children but intellectual disability is seen. Now scientists say that the genes responsible for these diseases have been discovered. Scientists have found in their research that a gene named CRNKL 1 is responsible for these deformities. This discovery of scientists has raised the hope of correcting these diseases through gene therapy in future.
The team of international researchers led by the University of Otago, New Zealand, has carried out this discovery. He has discovered a new genetic reason for a rare disorder related to brain development in children. This disorder severely affects the development and functionality of the brain of children. Research found that special changes in a gene called CRNKL1 can cause serious disorder, resulting in children, pre -birth and after microcephorial, pontocrebeller hypoplasia and severe intellectual disability. This discovery adds new lights to understand the complex process of genetic instructions required for the creation and maintenance of the brain.
New light on brain development
Louis Biknell, Associate Professor of Rare Disorder Genetics Laboratory in Otago’s Biochemistry Department, said, “Our body depends on an accurate process called Splissing to read and process genetic instructions from DNA.” This process makes the building blocks required for the body. When there is disturbance in this splissing, many genetic disorder causes. The new discovery shows its serious impact on the development of the brain. Published in the American Journal of Human Genetics, this research studied 10 families, out of which the CRNKL1 genes found genetic changes at the same place. All affected children had similar serious symptoms, showing a strong relationship between these genetic changes and disorder.
Dr. Sankalita Ray Das, the chief writer of research and post -deacter researcher, said, this research shows that CRNKL1 is important for healthy brain development. This discovery not only gives a new genetic cause of severe neurological disorder but also helps to understand how our genes control the development of the brain. He said that this discovery gives clarity to the affected families about the condition of their children and in the future prepares a base to understand why these genetic changes only affect the brain. This research is an important step towards treating and prevention of rare brain disorders. This discovery can open the way for the treatment of such children in future. Input -IANS
Excelled with Colors in Media Industry, Enriched more than 16 years of professional experience. Lakshmi narayan contributed to all genres viz print, television and digital media. He Professed His Contribution I …Read more
Excelled with Colors in Media Industry, Enriched more than 16 years of professional experience. Lakshmi narayan contributed to all genres viz print, television and digital media. He Professed His Contribution I … Read more