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Each of these categories is discussed briefly below.About 1 out of 150 live newborns has a detectable chromosomal abnormality.

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This article surveys the main categories of genetic disease, focusing on the types of genetic mutations that give rise to them, the risks associated with exposure to certain environmental agents, and the course of managing genetic disease through counseling, diagnosis, and treatment.

For full explanation of Mendelian and non-Mendelian genetics, genetic mutation and regulation, and other principles underlying genetic disease, Certain human diseases result from mutations in the genetic complement (genome) contained in the deoxyribonucleic acid (DNA) of chromosomes.

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Our web hosting company is based on the success of our customers; we empower them to succeed.A gene is a discrete linear sequence of nucleotide bases (molecular units) of the DNA that codes for, or directs, the synthesis of a…Most human genetic defects can be categorized as resulting from either chromosomal, single-gene Mendelian, single-gene non-Mendelian, or multifactorial causes.It must be emphasized that birth defects do not all have the same basis, and it is even possible for apparently identical defects in different individuals to reflect different underlying causes.Though the genetic and biochemical bases for most recognized defects are still uncertain, it is evident that many of these disorders result from a combination of genetic and environmental factors.Yet even this high incidence represents only a small fraction of chromosome mutations since the vast majority are lethal and result in prenatal death or stillbirth.

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