FH, family tree, pedigree, genogram Ans- Tools used in determining likelihood of genetic disorder in
family, inheritance patterns, and risk of recurrence in family members
U.S. Surgeon General's Family History Initiative Ans- Recommended that families know their family
history
Autosomal dominant conditions may be present in more than one generation and Ans- In up to 50% of
offspring when one parent is affected (such as Marfan syndrome)
Recessive conditions Ans- Appear only in one generation
Affects individuals who have two copies of a faulty gene, one from each (unaffected) parent Ans-
Recessive conditions (ex: CF, hemochromatosis)
X-linked disorders are caused by faulty genes on an Ans- X chromosome (fragile X syndrome, color
blindness)
Communication process used whenever there is a genetic risk and often involves offering a test that
could provide info about the genetic status of the person/implications for the family Ans- Genetic
counseling
Primary role is to offer info and support to persons concerned a out an illness that may have a genetic
basis Ans- Genetic Counselor
There are a total of Ans- 46 chromosomes, in 23 pairs
Chromosomes Ans- Structures of DNA
DNA Ans- Made up of two twisted, paired strands