Medical Genetics: Types of Genetic Changes
The human body has about 20,000 different genes in each cell. Genes are located on chromosomes, which are stick-shaped structures in the middle of the cell (nucleus). Each cell usually has 46 chromosomes grouped in 23 pairs. Each gene has a specific function. When a gene or chromosome is abnormal, it may cause health problems in the body.
Two types of genetic changes include:
What are chromosome abnormalities?
Chromosome abnormalities may be inherited from the parent or may occur with no family history. These are the most common:
This means there are more or fewer chromosomes than the normal number. Examples include:
Down syndrome (trisomy 21). Cells contain 3 copies of the 21st chromosome.
Turner syndrome. One of the 2 sex chromosomes is not present. This leaves a single X chromosome for 45 total chromosomes instead of 46.
This is when part of a chromosome is missing, or part of the DNA code is missing.
This is when a piece of a chromosome breaks off, turns around, then reattaches itself. Inversions can be passed down in families. They may or may not cause birth defects.
A ring chromosome is one where the ends of the chromosomes attach to each other to form a ring. Ring chromosomes can be passed down in families. They may or may not cause health problems.
This is when a piece of 1 or more chromosomes move to another location. This can occur either within the same chromosome or move to another chromosome. There are 2 main types:
Balanced translocation. This is when the DNA is equally exchanged between chromosomes. No DNA is lost or added. A person with a balanced translocation is generally healthy. But they may be at risk for passing on unbalanced chromosomes to a child.
Robertsonian translocation. This is a balanced translocation in which 1 chromosome joins the end of another.
This is when a person has 2 or more sets of cells that contain different genetic material.
What are single-gene changes?
A change in a single gene causes a defect or abnormality. Single-gene changes usually have a higher risk of being passed on to children. Single-gene changes can be:
This means the abnormality occurs when only 1 of the genes from 1 parent is abnormal. If the parent has the disorder, the baby has a 1 in 2 chance of inheriting it. Examples include:
This means the abnormality only occurs when both parents have a copy of an abnormal gene. If both parents are carriers, a baby has a 1 in 4 chance of having the disorder. Examples include:
Cystic fibrosis. This is a disorder of the glands that causes excess mucus in the lungs. It also causes problems with how the pancreas works and with how food is absorbed.
Sickle cell disease. This condition causes abnormal red blood cells that don’t carry oxygen normally.
Tay-Sachs disease. This is an inherited condition that causes the central nervous system to decline. The condition is fatal, usually by age 5.
The disorder is determined by genes on the X chromosome. Males are mainly affected and have the disorder. Daughters of men with the disorder are carriers of the trait and have a 1 in 2 chance of passing it to their children. Sons of women who are carriers each have a 1 in 2 chance of having the disorder. Examples include:
How genetic changes are passed along in a family
The way a gene is inherited can help determine the risk of it in a current or future pregnancy. The risk of having a baby with a birth defect from a genetic change increases if:
The parents have another child with a genetic disorder
There is a family history of a genetic disorder
One parent has a chromosome abnormality
The baby in the womb has abnormalities seen on an ultrasound
Families at risk for genetic diseases may want to talk with a certified genetic counselor. Making a chart of the family members and their health histories can help show risks for certain problems. Genetic counseling also helps parents understand the effects of a disorder and ways it may be prevented or treated.
Getting genetic testing
Each parent's DNA may need to be checked. This is done to learn about some genetic inheritance patterns. Prenatal testing can also be done to check the baby in the womb for problems. Testing may include:
Ultrasound. This test uses sound waves to look at how a baby in the womb is growing.
Chorionic villus sampling (CVS). This test uses a sample of tissues around the baby to look for problems.
Amniocentesis. This test uses a sample of the amniotic fluid from the sac around the baby to check for problems.
Noninvasive prenatal screening. This test involves taking a blood sample from the mother to look for chromosome differences, such as aneuploidy.
Carrier screening. This test uses a sample of blood from each parent to check if they carry genetic changes for certain genetic conditions.