Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.

Slides:



Advertisements
Similar presentations
Human Genetic Disorders
Advertisements

Human Inheritance Notes Ch Part II
NOTES 24 – Genetic Disorders and Hereditary Diseases
What’s Your Blood Type? A B AB O.
 What’s a “mutagen”?  What does a mutation do to DNA?  If a mutation affects a gene, then what might happen to the protein sequence?
Human Genetic Disorders
Chapter 12: Patterns of Heredity & Human Genetics
Pedigrees.
PEDIGREE CHARTS A family history of a genetic condition © 2007 Paul Billiet ODWSODWS.
Human Genetic Disorders
Human Genetics.
INHERITED GENETIC DISORDERS
This type of genetic disorder requires both parents to “donate” a defective gene.
Wake-up 1.A woman carrying hemophilia marries a man who is a hemophiliac. What percentage of their children will have hemophilia? 1.Cross a man heterozygous.
Chapter 12.  Humans have 46 chromosomes  44 are autosomes  22 pairs of homologous chromosomes  2 are sex chromosomes: X and Y  Females have two X.
Wake-up 1.A woman carrying hemophilia marries a man who is a hemophiliac. What percentage of their children will have hemophilia? 1.Cross a man heterozygous.
You already know… - A chromosome is a structure that carries genetic information Each cell normally has 23 pairs of chromosomes: 1 pair of sex chromosomes.
The Human Genome Karyotype  Mapped out picture of chromosomes arranged in their homologous pairs.  46 chromosomes in human genome  23 pairs on karyotype.
Human Heredity  This section explains what scientists know about human chromosomes, as well as the inheritance of certain human traits and disorders.
Human Genetics: Patterns of Inheritance for Human Traits.
Sex-linked Genetic Disorders & Autosomal Disorders Packet #41 Chapter #14.
Human Genetic Disorders
ABO Blood Groups and Genetic Disorders
Genetics Part 3 Modes of Inheritance
Genetic Disorders  Caused by mutations inherited from a parent  mutations are mistakes that are present in the DNA of virtually all body cells. VideoclipVideoclip.
Pedigrees and Karyotypes. Pedigree definition: Pedigree: a family history that shows how a trait is inherited over several generations Pedigrees are usually.
Inheritance and Human Genetics
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
Pedigree Used to show how a particular trait is passed from one generation to the next in a family.
Human Genetics: Patterns of Inheritance for Human Traits.
Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.
Inheritance of Traits: Pedigrees
Do Now Incomplete or Codominance? Human Genetics: Patterns of Inheritance for Human Traits.
Genetic Disorders.
Understanding Inheritance Patterns. -How to interpret Pedigree Charts.
Genetic Disorders. Caused by a harmful mutation (physical change of gene) Mutation originally occurs in gamete and is passed to future generations (inherited)
Human Genetic Disorders
Today’s Agenda…  Bellringer: Life Science Multiple Choice Questions  Discuss homework from last night  Notes on Human Genetic Disorders.
Human Genetic Disorders Notes. What causes genetic disorders? Mutations, or changes in a person’s DNA.
Topic: Modeling Inheritance Pedigree Charts. Related?  Cite evidence to indicate these two individuals are related.
Welcome 2/10-11/16 1. Turn in Quick Lab and Dihybrid Cross 2. Other Mendelian Genetics and Disorders Notes 3. Practice Non-Mendelian Genetics.
Autosomal Recessive Inheritance By: Joey Cisneroz 121.
Genetic Disorders Caused by ___?________ in the DNA mutations.
Section 2 Human Genetic Disorders. 1 st three terms…also in next 3 slides! Genetic disorder - an abnormal condition that a person inherits through genes.
Genetic Diseases & Disorders Biology Genetics Diseases outline Dominant 1. Huntington’s Recessive 1. Cystic fibrosis 2. Sickle-cell anemia 3. Tay-Sachs.
Sex-Linked Traits. Inheritance of Traits  X-linked Disorders - occur mainly in males because the mother usually donates the recessive allele and males.
Sex-linked Traits. Sex determination  Sex chromosomes – determines the sex of an individual YY XX  Males have X and Y  Two kinds of gametes  Female.
Pedigree Chart Notes Genetic Family Tree. What is a Pedigree?  A pedigree is a chart of the genetic history of family over several generations.  Scientists.
Human Genetic Disorders Human Genetics and Genetic Technology.
Chapter 12 Patterns of Heredity And Human Genetics.
Pedigrees 4/13/2010 Pedigrees The risks of passing on a genetic disorder to offspring can be assessed by genetic counseling, prenatal testing, and by.
More Patterns of Inheritance Autosomal inheritance – genes are located on the autosomes, same for both male and female Sex-linked inheritance – genes located.
Complex Patterns of Inheritance There are some exceptions to Mendel’s Laws.
Inherited Genetic Disorders & Pedigrees
Human Genetic Disorders
Human Genetics.
Warmup 5/12/16: Turn in U8 Qualifier and signed progress report to the folder at your station Next, complete the Pedigree Review Worksheet.
5.2 Human Genetic Disorders
How can you study human heredity?
Section 7-1 “Human genetics”
INHERITED GENETIC DISORDERS
Human Genetics Module 9.
GENETIC DISORDERS.
Human Genetics Module 9.
Pedigree Notes.
Pedigree Notes.
Genetic Disorders.
Example of Trait = Albinism
Pedigrees and Disorders
Key Concepts What are two major causes of genetic disorders in humans?
Presentation transcript:

Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents want to know if they are carriers of a particular disorder

Making a Pedigree  Female  Male  Married Couple  Siblings Filled in symbols indicate individual is affected with a disorder

Example of a Pedigree You Parents Aunts, Uncles Grandparents Brother Do any disorders run in this family??

Interpreting a Pedigree  What can you tell from a pedigree?  Whether a family has an autosomal or sex-linked disease or disorder  Autosomal disorder: appears in both sexes equally  Sex-linked disorder: allele is located only on the X or Y chromosome. Most sex-linked genes are on the X chromosome and are recessive  So who would have an X-linked disorder more often, boys or girls?  Whether a disorder is dominant or recessive

Is this disorder 1) autosomal or sex linked, 2) dominant or recessive? You Parents Aunts, Uncles Grandparents Brother Sex Linked! (in this case allele is recessive and located on the X chromosome)

Is this disorder 1) autosomal or sex linked, 2) dominant or recessive? You Parents Aunts, Uncles Grandparents Brother Autosomal dominant!

Is this disorder 1) autosomal or sex linked, 2) dominant or recessive? You Parents Aunts, Uncles Grandparents Brother Autosomal recessive!

Common Genetic Disorders  Color blindness  Sickle cell anemia  Cystic Fibrosis  Hemophilia  Huntington’s Disease For more info, go to:

Color Blindness  Deficiency to percieve colors  Problem with color- sensing pigments in certain nerve cells of the eye  About 1 in 10 men have some form of color blindness.  Sex-linked disorder

Sickle Cell Anemia  Disorder where abnormal hemoglobin (a protein inside red blood cells) is produced and warps red blood cells  Sickle cells deliver less oxygen to body’s tissues and can get stuck in small blood vessels  Recessive trait, tends to be seen in people of African or Mediterranean descent

Cystic Fibrosis  Recessive, autosomal disease  Life threatening, causes thick mucus to build up in various areas of the body (lungs, digestive tract, etc).  Tends to run in Caucasians, of Northern/Central European descent (1 in 29 Americans carry the allele)  Average life span in US for people with CF is 37, death usually caused by lung complications

Hemophilia  Bleeding disorder, where it takes a long time for blood to clot (body lacks proteins involved in clotting)  Sex-linked (carried on the X chromosome)  Treatment involves injection with missing clotting protein

Huntington’s Disease  Autosomal, dominant  Deterioration of brain tissue, usually begins between age 30 and 40.  No cure, but have medications to cope with symptoms  People usually die years after onset of degeneration