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Human Genetics Disorders

 A genetic disease is any disease produced by an irregularity in the genetic makeup of a separate. The genetic abnormality can variety from minuscule to major  from a discrete change in a single base in the DNA of a single gene to a gross chromosomal abnormality. Some people inherit genetic disorders from the parents, while developed changes or transformations in a pre-existing gene or collection of genes reason other genetic diseases Down syndrome typically, the nucleus of an individual cell contains 23 pairs of chromosomes, but Down syndrome occurs when the 21st chromosome is copied an extra time in all or some cells. DNA of a single gene to a gross chromosomal abnormality involving the addition or subtraction of a whole chromosome or set of chromosomes. Syndrome is an extremely rare genetic neurodevelopmental disorder in which there is a variation (mutation) in the KAT6A gene. Variations in the KAT6A gene can potentially cause a wide variety of signs and symptoms; how the disorder affects one child can be very different Deviations or mutations that occur in the DNA order of a single gene cause this type of inheritance