Genetic Disorders Flashcards
What is Down Syndrome caused by?
The individual has 3 copies of chromosome 21 which is caused by nondisjunction during meiosis.
Either the egg or the sperm has 2 copies instead of 1 of chromosome 21.
What does sporadic trisomy mean?
It means the trisomy is not inherited
True or False: You get 100% transfer over of genes
False, sometimes you don’t get 100% transfer over of genes
What are two factors that impact how symptoms of Down Syndrome show in individuals?
Environment & genetic background
List symptoms for Down Syndrome
- Intellectual Disability (100%)
- Congenital Heart Defect (40%)
- Hypotonia
- Atlantoaxial instability (neck) (12%)
- Hyperthyroidism/goiter (over active thyroid can cause metabolism issues & weight loss)
- Character facial features
- Increased incidence of Leukemia (1%)
- Male infertility
- Female significantly reduced fertility
How can an extra chromosome cause a wide range of phenotypic effects?
- Chromosomes transmit genetic information
- The type & amount of genetic material is important for normal development
Describe Tiploidy 69
In this syndrome you have a full extra set of chromosomes
-Usually caused by paternal chromosomes
- Not compatible with long term survival
- 2% of all conceptions
- 20% of all chromosomally abnormal miscarriages
- 3% of triploid conceptuses survive to be recognized
- Partial hydatidiform mole, usually associated with triploidy
Describe the etiology of Triploidy 69
- No association with maternal age
- 69% are paternally derived due to double fertilization
- Remaining are failure of meiosis 2 resulting in diploid egg
Explain why it is important that meiosis is a reduction division.
We need haploid gametes in order to live normal lives.
What would occur to successive generations if it was not a reduction division?
Would this result in viable offspring?
Each generation would end up with excessive chromosomes
-No
What does recurrent microdeletions & duplications result in?
nonhomologous recombination which results in unequal crossing over
What is attributed to extra gene regions?
Phenotype
Which disorder is associated with cat-eye syndrome?
Partial Tetrasomy 22q11
Describe 22q11 syndrome
Highly variable-can be mosaic
Supernumerary marker chromosome involving two copies of 22q11
Symptoms include: cat-eyes
-down slanting palpebral fissures
-change in Iris and anal atresia with fistula
What is a Dicentric chromosome?
A chromosome with 2 centromeres