Genetics and genomics for healthcare www.geneticseducation.nhs.uk © 2014 NHS National Genetics Education and Development Centre Recognising patterns of.

Slides:



Advertisements
Similar presentations
Pedigrees Who do we inherit our traits from? DO YOU LOOK LIKE YOUR AUNT OR UNCLE? DO YOU AND YOUR COUSIN SHARE TRAITS?
Advertisements

Collecting family history information This presentation can be used as part of Lesson Plan 3 Taking and Drawing a Family History. It can also be used with.
Genetics and inheritance Questions with true or false answers
Genetics and genomics for healthcare © 2014 NHS National Genetics and Genomics Education Centre Why is genetics relevant to.
Genetics Spring 2015 Chromosomes and Sex-Chromosomes Inheritance I.
Genetics and genomics for healthcare © 2013 NHS National Genetics and Genomics Education Centre How to draw a family history.
X-linked dominant inheritance: the basics a tutorial to show how the genes segregate to give the typical pedigree pattern Professor P Farndon, Clinical.
Sex-linked traits. Sex chromosomes carry genes that code for traits other than gender. Traits determined by genes on the X chromosome are called sex-linked.
FOR FRESHERS Mendelian Inheritance. Mendelian inheritance There are two alleles of a gene on different sister chromosomes. Dominant alleles trump recessive.
Pedigrees.
Human Genetics Chapter 14.
Inborn Errors of Metabolism BCH 451 Dr. Amina ElGezeery.
Genetics and genomics for healthcare © 2013 NHS National Genetics and Genomics Education Centre Passing on genetic information.
Genetics and Dementia – what do relatives want to know? Candy Cooley NHS National Genetic Awareness Lead Genetics and genomics for healthcare
Autosomal recessive inheritance Risks to children where a parent is affected: the basics a tutorial to show how the genes segregate to give the typical.
Single gene disorder pedigree proband: affected individual that initially comes to light kindred: relatives outside of the immediate nuclear family siblings:
Heredity Study Guide Answer Key.
Pedigrees & Genetic Analysis. Learning Objectives By the end of this class you should understand: The purpose of a pedigree How to read and interpret.
Do Now : Think-Pair-Share For a height characteristic when tall is dominant What would be the phenotypic ratio for offspring of heterozygous and homozygous.
Pedigree Charts The family tree of genetics.
Pedigrees A pedigree is a diagram of family relationships that uses symbols to represent people and lines to represent genetic relationships. In a pedigree,
HUMAN GENETICS. Objectives 2. Discuss the relationships among chromosomes, genes, and DNA. 2.8 Examine incomplete dominance, alleles, sex determination,
5.3 Tracking Inheritance Pages
Chapter 12 Review Sheet. What are the sex chromosomes? X Y.
The Human Genome Chapter 14.
Pedigree Charts The family tree of genetics. Overview I.What is a pedigree? a. Definition b. Uses II. Constructing a pedigree a. Symbols b. Connecting.
Genetics and genomics for healthcare © 2014 NHS National Genetics and Genomics Education Centre Genetics and Genomics: Alert,
Pedigree Charts The family tree of genetics Created by Lauren Almaguer, CDC Science Ambassador, 2004.
A family history of a genetic condition
Chapter 14 - The Human Genome
Inheritance of Traits: Pedigrees
Genetics and genomics for healthcare © 2013 NHS National Genetics and Genomics Education Centre Passing on genetic information.
Understanding Genetic Testing
Human Genetics. How many pairs of chromosomes are in each of our body cells? A.32 B.23 C.46 D pairs! This is 46 total; we get 23 from mom & 23 from.
1 Human Genetics: Pedigrees. Pedigree Looks at family history and how a trait is inherited over several generations and can help predict inheritance patterns.
Lecture 8 Dr. Attya Bhatti
Genetic disorders can be due to any of the following factors: A. Monogenetic Disorders: Caused by a mutation in a single gene 1. Autosomal recessive alleles:
Human Genetics Chapter 12
PEDIGREES Tracing traits through generations 1. What is a Pedigree?  a Pedigree is a chart that traces the occurrence of a trait through several generations.
5.3 Tracking Inheritance Pages
Pedigree Charts The family tree of genetics. Overview I.What is a pedigree? a. Definition b. Uses II. Constructing a pedigree a. Symbols b. Connecting.
A genetic disorder is an illness caused by one or more abnormalities in the genome, especially a condition that is present from birth (congenital). Most.
Javad Jamshidi Fasa University of Medical Sciences, October 2015 Session 4 Medical Genetics Part 1 Patterns of Inheritance.
Pedigree Charts The family tree of genetics. What is a Pedigree?  A pedigree is a chart of the genetic history of family over several generations.
What is a Pedigree… And Nooooo it’s not Dogfood. Biology I Searcy Ninth Grade Center.
Sex Determination In humans, the X and Y chromosomes control the sex of offspring. Outcome is always 50% chance of a male, and 50% chance of a female Female.
The family tree of genetics
Pedigree Charts The family tree of genetics. Learning Objective I can use the correct symbols to put together a pedigree chart I can predict a genotype.
4 Human inheritance (2015). Human inheritance In this lesson we will describe the inheritance of traits due to dominant and recessive genes, located on.
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.
The family tree of genetics
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.
Pedigree Charts The family tree of genetics. Overview I.What is a pedigree? a. Definition b. Uses II. Constructing a pedigree a. Symbols b. Connecting.
Example of Trait = Albinism
Pedigree Charts The family tree of genetics. What is a Pedigree?  A pedigree is a chart of the genetic history of family over several generations. 
Pedigree.
Unit 2:.
Pedigrees in Human Genetics
Inheritance Pedigree Analysis.
Two copies of each autosomal gene affect phenotype.
Unit 3.
Sex-Linked: Following the X & Y Chromosomes
Pedigree Lecture 7.
Different mode and types of inheritance
Two copies of each autosomal gene affect phenotype.
Pedigrees & Karyotypes
Sex-Linked Following the X & Y Chromosomes
4.2 Understanding Inheritance
Take out pedigree homework
Pedigree Practice Mrs. Henning.
Presentation transcript:

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Recognising patterns of inheritance quiz

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre This quiz was designed to help in identifying the different patterns of inheritance by analysing how people with a condition are related to each other. In practice, additional information may be available: – For instance, the diagnosis itself may confirm a mode of inheritance. Then, the pedigree can be inspected to see if the pattern fits with that expected. – Some combinations of clinical features may suggest that the condition is due to an anomaly of chromosomes.

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Introduction There are 10 genetic family histories (illustrated as pedigrees) in this quiz. The first slide for each family gives the pedigree and invites you to choose the most likely mode of inheritance from a list of 4 or 5 alternatives. The second slide for each family gives the answer we think most likely and gives explanations in the notes pane as to why some of the other alternatives are not appropriate. In the explanations, we often use the term “affected people”. Patients much prefer the term “people with the condition” but we use the term “affected” here as a shorthand form to save space.

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Additional resources Animated presentations explaining the single gene modes of inheritance can be found here: healthcare-educators/presentations healthcare-educators/presentations Video animations explaining single gene modes of inheritance can be found via the following page: des-of-inheritance/single-gene-conditions des-of-inheritance/single-gene-conditions

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Some reminders before you begin The internationally agreed symbols for males and females are squares and circles respectively. A symbol is coloured in if the person has a condition. Small triangles are miscarriages or spontaneous abortions. The sex chromosomes of males are XY; females have XX sex chromosomes. Mitochondria come from the egg and not the sperm.

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Questions to consider when looking at a pedigree Do males and females have the condition? Are there roughly equal numbers of males and females with the condition? Are there people in each generation with the condition? Do people with the condition have children with the condition? Do people without the condition have children with the condition?

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 1 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Chromosomal translocation b. Autosomal dominant c. X-linked dominant d. Mitochondrial e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 1 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Chromosomal translocation b. Autosomal dominant c. X-linked dominant d. Mitochondrial e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 2 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Y linked b. Autosomal recessive c. Autosomal dominant d. X-linked recessive e. X-linked dominant

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 2 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Y linked b. Autosomal recessive c. Autosomal dominant d. X-linked recessive e. X-linked dominant

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 3 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? The affected person has a metabolic disorder caused by an enzyme deficiency. The disorder causes learning disabilities, coarsening of the facial features and skeletal anomalies. a. Autosomal dominant b. Autosomal recessive c. X-linked recessive d. Multifactorial

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 3 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? The affected person has a metabolic disorder caused by an enzyme deficiency. The disorder causes learning disabilities, coarsening of the facial features and skeletal anomalies. a. Autosomal dominant b. Autosomal recessive c. X-linked recessive d. Multifactorial

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 4 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Reciprocal chromosomal translocation b. Autosomal dominant c. X-linked dominant d. Mitochondrial e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 4 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Reciprocal chromosomal translocation b. Autosomal dominant c. X-linked dominant d. Mitochondrial e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 5 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? Two people were born with spina bifida but are otherwise healthy. a. X-linked recessive b. Mitochondrial c. Autosomal dominant d. Multifactorial

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 5 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? Two people were born with spina bifida but are otherwise healthy. a. X-linked recessive b. Mitochondrial c. Autosomal dominant d. Multifactorial

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 6 The children with the condition in this family have multiple congenital anomalies and developmental delay. Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Reciprocal chromosomal translocation b. Autosomal dominant c. X-Linked recessive d. Mitochondrial e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 6 The children with the condition in this family have multiple congenital anomalies and developmental delay. Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Reciprocal chromosomal translocation b. Autosomal dominant c. X-Linked recessive d. Mitochondrial e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 7 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. X-linked dominant b. Autosomal dominant c. Multifactorial d. X-Linked recessive e. Reciprocal chromosomal translocation

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 7 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. X-linked dominant b. Autosomal dominant c. Multifactorial d. X-Linked recessive e. Reciprocal chromosomal translocation

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 8 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Autosomal dominant b. Autosomal recessive c. X-Linked recessive d. Y-Linked e. X-Linked dominant

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 8 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. Autosomal dominant b. Autosomal recessive c. X-Linked recessive d. Y-Linked e. X-Linked dominant

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 9 Which of the modes of inheritance is the most likely based on the pattern of people with the medical condition in this family? a. X-linked recessive b. Reciprocal chromosomal translocation c. Mitochondrial d. New mutation causing a dominant condition e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 9 Which of the modes of inheritance is the most likely based on the pattern of people with the medical condition in this family? a. X-linked recessive b. Reciprocal chromosomal translocation c. Mitochondrial d. New mutation causing a dominant condition e. Autosomal recessive

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 10 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. X-linked dominant b. Autosomal dominant c. X-linked recessive d. Mitochondrial e. Y-linked

Genetics and genomics for healthcare © 2014 NHS National Genetics Education and Development Centre Family 10 Which of the modes of inheritance is the most likely based on the pattern of people with the condition in this family? a. X-linked dominant b. Autosomal dominant c. X-linked recessive d. Mitochondrial e. Y-linked