Huntington's and Polydactyly Disease L/O: To understand how genetic inheritance of Huntington's and polydactyly occurs Starter Recap: If a mother is a.

Slides:



Advertisements
Similar presentations
1. Identify the process being illustrated?
Advertisements

Andrew Novoa and Thea De Guzman 2/1/10 Per. 3
Warm-up What do you already know about chromosomes? Tell me at least one thing!
14.1 Human Chromosomes What makes us human? What makes us different from other animals such as a chimpanzee? About 1% of our DNA differs from a chimp.
NOTES 24 – Genetic Disorders and Hereditary Diseases
Year 10 – Genetics and Biotechnology (Biology) Genetic disorders.
GENETIC DISORDERS & DISEASES. Types?  Dominant  Recessive  Sex Linked  Chromosomal  Mutagens?
Mendel ( ) Mendel studied inheritance in peas. His idea was that organisms passed on separate characteristics via “inherited factors” (we now call.
By: Dasia Davis Gabriella Mirenda Lorena Sposato.
Human Genetics Chapter 14 in the Textbook.
Noadswood Science,  To understand how some diseases can be inherited Sunday, August 16, 2015.
Inherited Conditions (Genetic Disorders). I can describe at least two genetic disorders (diseases). I can predict the likelihood of a child inheriting.
INHERITED GENETIC DISORDERS
Period 2.  Polydactyly is a condition in which a person has more than five fingers per hand or five toes per foot.  Polydactyly occurs in the.
IB Genetic disorders © Oxford University Press 2011 Genetic disorders.
14-19 Learning Core Development Programme Laura Blacoe Connah’s Quay High School.
Genetics and Heredity. Genetics Genetics is the study of heredity It looks at understanding the biological properties that are transmitted from parent.
Genetic Pedigree Diagrams. What are genetic pedigree diagrams? Show how an inherited trait (characteristic) runs in a group of related individuals. You.
Unit 4: Heredity and Development 4-2 Mendelian Genetics.
Human Genetics: Patterns of Inheritance for Human Traits.
Genetics Part 3 Modes of Inheritance
Thursday 2/2 How many copies of the chromosome for skin color do you have? Why do you have that many? What is similar and what is different about the.
Genetic Diseases L.O: To understand how some genetic diseases can be inherited Starter: list as many inherited diseases that you can think of.
Genetics Part II: Probability and Pedigree
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
Human Pedigrees 12.3 pg 255. Pedigrees  Family tree that records and traces the occurance of a trait in a family.  Analyze patterns  Applies Mendel’s.
A. albinism B. cystic fibrosis C. galactosemia D. Tay-Sachs 1. Identify the disease characterized by the absence of melanin. Complex Inheritance and Human.
Human Genetics: Patterns of Inheritance for Human Traits.
Patterns of Heredity Pedigrees March 19, Section Objectives – page 309 Interpret a pedigree. Section Objectives: Identify human genetic disorders.
Do Now Incomplete or Codominance? Human Genetics: Patterns of Inheritance for Human Traits.
Genetic Disorders By: Tanner and Jack.
What is a mutation?. Genetic Disorders Make a list of all the genetic disorders you have heard of – do you know what causes them?
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)
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.
Sickle Cell Andrew Novoa and Thea De Guzman 2/1/10 Per. 3.
Genetic Disorders Caused by ___?________ in the DNA mutations.
Unit 2 – Pedigrees.
IB Inheriting genetic disorders © Oxford University Press 2011 Inheriting genetic disorders.
Chapter 14 Test Prep. _____ 2. If the allele for having a white forelock is dominant, family members WITHOUT a white forelock are a. homozygous recessive.
Honors Biology- Chapter 14. The Human Genome Project  Completed in 2003  13 year project  discovered all the estimated 20,000-25,000 human genes 
B1 Smart Teach Foundation Session 3. Keywords Key wordDefinition NucleusPlace inside a cell that contains the DNA (chromosomes). DNAA molecule found in.
Sex-Linked Traits. Inheritance of Traits  X-linked Disorders - occur mainly in males because the mother usually donates the recessive allele and males.
Mills Biology. California State Standards  2.c Students know how random chromosome segregation explains the probability that a particular allele will.
Genetic Disorders Cystic Fibrosis
Genetics: Inheritance. Meiosis: Summary  Diploid Cells (2n): Cells with two sets of chromosomes, (aka “homologous chromosomes”)  One set of chromosomes.
What do you know? Meiosis & mitosis? Inheritance? Cystic Fibrosis? Polydactly?
Complex Inheritance Patterns
Single Gene Inheritance
Human Genetics: Patterns of Inheritance for Human Traits
Difference between a monohybrid cross and a dihybrid cross
Human Heredity.
Human Heredity.
Extending Mendelian genetics
5.3- Following Patterns of Inheritance in Humans
INHERITED GENETIC DISORDERS
Inheriting a Genetic Disorder
Human Pedigrees Inheritance Patterns.
& Human Heredity January 6th/7th, 2008
Presented by Kesler Science
Genetics Chapter 10—pages
What gender is XX female.
Presented by Kesler Science
Inherited Disorders Effective Participator Reflective Learner Self
Chapter 10 assessment.
Inherited Disorders.
Human Genetics.
Presentation transcript:

Huntington's and Polydactyly Disease L/O: To understand how genetic inheritance of Huntington's and polydactyly occurs Starter Recap: If a mother is a carrier and a father has cystic fibrosis, draw out the chances of having the conditions CORE: Effective Participators Success Criteria: C – State what Huntington's and polydactyly are B – Describe the symptoms of Huntington's and polydactyly and how they occur A – Explain the genetic basis for Huntington's and polydactyly A* - Predict the likelihood of inheritance of Huntington's and polydactyly KEY WORDS Huntingtonsgenes recessive dominant expressed polydactyly

Huntington's Chorea Huntington’s Disease = genetic disorder of the nervous system What symptoms might this cause? Look at the questions and answer these as you watch

Huntington’s Disease

Huntington’s Genetics How does Huntington’s continue throughout generations?

Quick check… 1.What type of disease is Huntington’s disease? 2.What are some of the external symptoms of Huntington's disease? 3.Who is affected by huntington’s disease? 4.What chromosome is affected in Huntington’s disease? 5.What are the internal symptoms?

How do you inherit Huntington’s? Huntington’s genes are dominant, so you only need one parent to have it to inherit the condition Allele for Huntington's = H Normal Allele = h Complete the genetic cross for the following three situations: a)Both parents have the disorder in both alleles b)One parent has the condition and the other does not Dominant = stronger gene that is expressed How do you think the disease comes to be passed on?

Polydactyly Polydactyly = genetic disorder where babies are born with extra fingers or toes The inheritance sequence is the same as for Huntington’s as it is a dominant disorder Complete the genetic cross for the following two situations: a)Both parents have the disorder in both alleles b)One parent has the condition and the other does not

Sickle Cell Anaemia Caused by a recessive allele (s) Causes red blood cells to change shape – can be trapped in blood vessels & anaemia

Sickle Cell Anaemia Symptoms: -Breathlessness -Lack of energy -Tired -Affected children fail to grow -Pain and death of tissue -Block blood vessels

Sickle Cell Anaemia What is the advantage of being heterozygous for sickle cell anaemia in certain regions?

Dimples The allele for dimples (D) is dominant over the allele for no- dimples (d). D d d d Dd dd Dd dd Probability of a child with dimples 50%

Albinism The allele for normal melanin (M) is dominant over the allele for albinism (m). Mm M m MM Mm mm Probability of a child with albinism 25%

Fact Page on Huntington’s or polydactyly for a doctors surgery Success Criteria: C – State what Huntington's and polydactyly are B – Describe the symptoms of Huntington's and polydactyly and how they occur A – Explain the genetic basis for Huntington's and polydactyly A* - Predict the likelihood of inheritance of Huntington's and polydactyly Huntington’s genes are dominant, so you only need one parent to have it to inherit the condition

Apply your knowledge… Complete the examination question to check your understanding of the disease. Success Criteria: C – State what Huntington's and polydactyly are B – Describe the symptoms of Huntington's and polydactyly and how they occur A – Explain the genetic basis for Huntington's and polydactyly A* - Predict the likelihood of inheritance of Huntington's and polydactyly