CHAPTER 12 HUMAN GENETICS. Chromosomal Abnormalities 1 infant in 200 newborns has a chromosomal...
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Transcript of CHAPTER 12 HUMAN GENETICS. Chromosomal Abnormalities 1 infant in 200 newborns has a chromosomal...
![Page 1: CHAPTER 12 HUMAN GENETICS. Chromosomal Abnormalities 1 infant in 200 newborns has a chromosomal abnormality 28% of first trimester miscarriages have a.](https://reader035.fdocuments.in/reader035/viewer/2022062517/56649e8b5503460f94b90792/html5/thumbnails/1.jpg)
CHAPTER 12HUMAN GENETICS
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Chromosomal Abnormalities
• 1 infant in 200 newborns has a chromosomal abnormality • 28% of first trimester miscarriages have a chromosomal abnormality
• Abnormalities in larger chromosomes don’t usually survive
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Color BlindnessCause:
Mutation in gene on X chromosome
Symptoms:• More common in males
(8% of males are colorblind)• Can’t distinguish certain
colors • Most common = red/green
Can you see the numbers and shapes?
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HemophiliaCause:
change in gene on X chromosome that codes for blood clotting protein
Symptoms:• More common in males• Internal and external bleeding•Can result in death•Transfusions & hospitalization are required frequently to stop bleeding!
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Cystic Fibrosis• Mutation in gene on chromosome 7
• Symptoms: – More common in Caucasians
– Make extra thick mucous in lungs and pancreas which leads to respiratory and digestive complications
– Salty skin is clue
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Achondroplasia(Dwarfism)
Cause: (Autosomal DOMINANT- found on chromosome 4)
Most new mutations in egg or sperm cell, but can be inherited from parent with gene
•1 in 20,000 births
•200,000 “little people” worldwide
•Normal size torso; short arms and legs
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DeletionPiece of DNA code is lost
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Wolf-Hirschhorn syndrome
• Deletion on arm of chromosome 4
• Mental retardation
• Large low set ears
• Club feet
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Cri-du-chat “cry of the cat”• Deletion on arm of chromosome 5• 1 in 50,000 births• More common in girls
• Mewing cry in infancy• Mental retardation
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Prader-Willi Syndrome • Deletion in chromosome 15
• Feeding problems: poor weight gain in infancy, won’t eat
• Ages 1-6 excessive, rapid weight gain
Victor at age 1 Victor at age 2
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Duchenne Muscular Dystrophy
Symptoms:• Deletion in gene on X chromosome• 1 in 3500 male births• Appears before age 5• Progressive muscle weakening• Most in wheelchair by age 13• Eventually lethal
Jerry Lewis telethon
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Non-disjunctionA homologous pair sticks together and doesn’t
separate at MEIOSIS.
One cell gets 2 copies of the chromosome the other cell gets none.
Monosomy- 1 chromosomeTrisomy- 3 chromosomes
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Down’s syndrome (trisomy 21)•Most common chromosomal abnormality
•1 in 660 births
•Similar facial features
•Slanted eyes
•Protruding tongue
•Mental retardation
•Risk increases with age of mom
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Patau syndrome (trisomy 13)•1 in 7000 births (rare)
•Cleft lip & palate•Eye abnormalities
(too small or missing)
low set ears
polydactyly
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Kleinfelter syndrome XXy
•1 in 1000 births
•Male = XXy
•Average to slight decrease in intelligence
•Small testes/can’t have children
•Usually not discovered until puberty when don’t mature like peers
•Has breast tissue & poor beard growth
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Turner’s syndrome (X)
• 1 in 5000 births• Female = X• Small size• Slightly decreased
intelligence• Hearing loss common• Undeveloped
ovaries/can’t have children
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Xyy syndrome
• Xyy males• Taller, more aggressive• Some early studies showed
greater incidence of Xyy males in prison populations than in the normal population
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Substitutions
Can YOU find the difference?
the fat cat ran and ran
the fat rat ran and ran
Sickle Cell Anemia is caused by this.
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Sickle Cell Anemia
•Substitution on chromosome #11
A is changed to T
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Insertion (addition)Extra Piece of DNA is added to code
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Huntington’s • Insertion at end of gene on chromosome 4
• Degenerative brain disorder
• Symptoms appear at age 30-40 (Usually after having children) • Lose ability to walk, think, talk, reason
• 50/50 chance of passing it to childNow there is a test to tell if you have the gene before symptoms appear.Would you want to know?
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How can we detect disorders?
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Karyotype
•Can tell missing/extra chromosomes•Gender•Some deletions/additions
What is wrong with
this karyotype?
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Amniocentesis•Insert needle into sac and withdraw fluid containing baby’s cells
•Done at 14-16 weeks
•Can detect:•Cystic Fibrosis•Huntington’s•missing/extra chromosomes
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The End.