Genetics research studies how individual genes or groups of genes are involved in health and disease. Understanding genetic factors and genetic disorders is important in learning more about preventing birth defects, developmental disabilities, and other unique conditions among children.
Some genetic changes have been associated with an increased risk of having a child with a birth defect or developmental disability. Genetics also can help us understand how birth defects and developmental disabilities happen.
How We Get Our Genes
People get (inherit) their chromosomes, which contain their genes, from their parents. Chromosomes come in pairs and humans have 46 chromosomes, in 23 pairs. Children randomly get one of each pair of chromosomes from their mother and one of each pair from their father. The chromosomes that form the 23rd pair are called the sex chromosomes. They decide if a person is male or female. A female has two X chromosomes, and a male has one X and one Y chromosome. Each daughter gets an X from her mother and an X from her father. Each son gets an X from his mother and a Y from his father.
Genetic disorders can happen for many reasons. Genetic disorders often are described in terms of the chromosome that contains the gene. If the gene is on one of the first 22 pairs of chromosomes, called the autosomes, the genetic disorder is called an autosomal condition. If the gene is on the X chromosome, the disorder is called X-linked.
Genetic disorders also are grouped by how they run in families. Disorders can be dominant or recessive, depending on how they cause conditions and how they run in families.
For recessive diseases, both copies of a gene must have a DNA mutation in order to get one of these diseases. If both parents have one copy of the mutated gene, each child has a 25% chance of having the disease, even though neither parent has it. In such cases, each parent is called a carrier of the disease. They can pass the disease on to their children, but do not have the disease themselves.
Single Gene Disorders
Some genetic diseases are caused by a DNA mutation in one of a person’s genes. For example, suppose part of a gene usually has the sequence TAC. A mutation can change the sequence to TTC in some people. This change in sequence can change the way that the gene works, for example by changing the protein that is made. Mutations can be passed down to a child from his or her parents. Or, they can happen for the first time in the sperm or egg, so that the child will have the mutation but the parents will not. Single gene disorders can be autosomal or X-linked.
For example, sickle cell disease is an autosomal single gene disorder. It is caused by a mutation in a gene found on chromosome 11. Sickle cell disease causes anemia and other complications. Fragile X syndrome, on the other hand, is an X-linked single gene disorder. It is caused by a change in a gene on the X chromosome. It is the most common known cause of intellectual disability and developmental disability that can be inherited (passed from one generation to the next).
Different Number of Chromosomes
People usually have 23 pairs of chromosomes. But, sometimes a person is born with a different number. If a person has an extra chromosome it is called trisomy. If a person has a missing chromosome it is called monosomy.
For example, people with Down syndrome have an extra copy of chromosome 21. This extra copy changes the body’s and brain’s normal development and causes intellectual and physical problems for the person. Some disorders are caused by having a different number of sex chromosomes. For example, people with Turner syndrome usually have only one sex chromosome, an X. Women with Turner syndrome can have problems with growth and heart defects.
Changes in Chromosomes
Sometimes chromosomes are incomplete or shaped differently than usual. When a small part of a chromosome is missing, it is called a deletion. If it has moved to another chromosome, it is called a translocation. If it has been flipped over, it is called an inversion.
For example, people with Williams syndrome are missing a small part of chromosome 7. This deletion can result in intellectual disability and a distinctive facial appearance and personality.
A complex disease is caused by both genes and environmental factors. Complex diseases also are called multifactorial. Many birth defects and developmental disabilities are complex conditions. For example, while some orofacial clefts are associated with single gene disorders, the majority most likely are caused by changes in several genes acting together with environmental exposures.
For More Information
- Genes in Lifeexternal icon
Genes in Life was created by Genetic Alliance to answer your questions about health and genetics.
- GeneEd Webexternal icon
GeneEd Web, developed and maintained by the National Library of Medicine (NLM) and the National Human Genome Institute (NHGRI), National Institutes of Health (NIH), is a safe and useful resource for students and teachers in grades 9 – 12 to learn genetics.
- G2C2 Genetics/Genomics Competency Center for Educatorsexternal icon
The mission of G2C2 is to provide high quality educational resources for group instruction or self-directed learning in genetics/genomics by health care educators and practitioners.
- Educational Materials About Genetics and Genomicsexternal icon
This National Human Genome Research Institute website offers a talking glossary of genetic terms, fact sheets, and other genetics-related resources.
- Learn.Genetics: Genetic Science Learning Center at the University of Utahexternal icon
This is the website for the Genetic Science Learning Center, a science and health education program located in the midst of the bioscience research being carried out at the University of Utah.
- Six Things Everyone Should Know About Geneticsexternal icon
This American Society of Human Genetics website provides basic genetics information and resources.
DNA, the genetic instructions in all living things, is packaged into small units called chromosomes. A chromosome contains a single, long piece of DNA with many different genes. Every human cell contains 23 pairs of chromosomes.
A gene is a part of DNA (the genetic instructions in all living things). People inherit one copy of each gene from their mother and one copy from their father. The genes that a person inherits from his or her parents can determine many things, like what a person will look like and whether the person might have certain diseases.
DNA is made up of two strands that wind around each other and looks like a twisting ladder. A DNA strand is made up of four different “bases” arranged in different orders. These bases are T (thymine), A (adenine), C (cytosine), and G (guanine). DNA is “read” by the order of the bases, that is by the order of the Ts, Cs, Gs, and As. The specific order, or sequence, of these bases determines the exact information carried in each gene (for example, instructions for making a specific protein). DNA has the same structure in every gene and in almost all living things.
A mutation is a change in a DNA sequence. DNA mutations in a gene can change what protein is made. Mutations present in the eggs and sperm (germline mutations) can be passed on from parent to child, while mutations that occur in body cells (somatic mutations) cannot be inherited.
A protein is made up of building blocks called amino acids. The main role of DNA is to act as the instructions for making proteins. It is actually proteins that make up most of the structures in our bodies and perform most of life’s functions. For example, proteins make up hair and skin. Proteins in our eyes change shape in response to light so we can see. Proteins in our bodies break down food. Proteins are made in cells and are the major parts of cells, which are the vital working units of all living things.
- Environmental Factors
Environmental factors can include exposures related to where we live as well as behaviors such as smoking and exercise and cultural factors such as foods that we eat.