Definition
A pedigree is a family tree or chart made of symbols and lines that represent a patient's genetic family history. The pedigree is a visual tool for documenting biological relationships in families and the presence of diseases. Pedigree analysis is an assessment made by a medical professional about genetic risk in a family.
Purpose
Pedigrees are most often constructed by medical geneticists or genetic counselors. People are referred to genetic professionals because of concern about the presence of a genetic condition in a family member. Pedigree analysis can help identify a genetic condition running through a family, aids in making a diagnosis, and aids in determining who in the family is at risk for genetic conditions. During pedigree construction, the family's beliefs about the cause for a genetic disease or emotional issues related to a diagnosis may be revealed. For
Pedigree symbols
A standard set of symbols has been established for use in creating pedigrees. Some of the most commonly used symbols are shown in this entry. When a person is affected with a birth disorder, mental retardation, or other health problems, the individual is shaded or marked. If more than one condition is present in a family, different identifying marks should be made. A key to decipher these markings should also be included on the pedigree. The meaning of each horizontal and vertical line is also shown.
Information obtained
A typical pedigree is made of information about three generations of a family. The consultand is the person seeking genetic evaluation, counseling, or testing. The proband in a family is the person in a family affected with a genetic disorder. Beginning with the consultand, questions should be asked about the health of first, second, and third degree relatives. First-degree relatives are children, parents, and siblings. Second-degree relatives are half siblings, nieces, nephews, aunts and uncles, grandparents, and grandchildren. Third-degree relatives are first cousins. Important information to obtain on both sides of the family includes:
- ages or dates of birth
- presence of any birth disorders, learning problems, chronic illnesses, surgeries, or medical treatments
- presence of specific features of a disease if the condition is suspected in the family
- genetic testing results if previously performed in the family
- cause of death for deceased family members
- pregnancy losses, stillbirths, or infant deaths and causes
- infertility in the family
- ethnic background of the families
- consanguinity
It is important to establish the accuracy of information given by patients. Therefore, medical records are often requested in order to provide accurate risk assessment.
Author Info: Sonja Rene Eubanks MS, CGC, The Gale Group Inc., Gale, Detroit, 2002

