What is the inheritance pattern (e.g., autosomal, sex-linked, dominant, recessive, etc.)?

Similar documents
Lesson Overview. Human Genetic Disorders. Lesson Overview Human Genetic Disorders

Lesson Overview. Human Genetic Disorders. Lesson Overview Human Genetic Disorders

Human Genetic Disorders. Lesson Overview. Lesson Overview Human Genetic Disorders

Cystic Fibrosis. Parkland College. Monica Rahman Parkland College. Recommended Citation

Respiratory Pharmacology: Treatment of Cystic Fibrosis

FACTS ABOUT. Cystic Fibrosis. What Is Cystic Fibrosis. What Are the Signs and Symptoms of CF?

Lab Activity Report: Mendelian Genetics - Genetic Disorders

PATIENT EDUCATION. Cystic Fibrosis Carrier Testing

Human Genetic Diseases (Ch. 15)

Human Genetic Diseases. AP Biology

When bad things happen to good genes: mutation vs. selection

Cystic Fibrosis. Na+ 2Cl - K+ Na+ Na+

Diseases of the gastrointestinal system. H Awad Lecture 2: small intestine/ part 2 and appendix

Each person has a unique set of characteristics, such as eye colour, height and blood group.

Human Genetic Disorders

Cystic Fibrosis. Presented by: Chris Belanger & Dylan Medd

Human Genetic Diseases. AP Biology

MULTIPLE CHOICE QUESTIONS

Evaluation of Patients with Diffuse Bronchiectasis

Cystic Fibrosis. Jennifer McDaniel, BS, RRT-NPS

Genetic Disorders. Students must provide an explanation for all problems. Students must have parent signature prior to submission.

Tay Sachs, Cystic Fibrosis, Sickle Cell Anemia and PKU. Tay Sachs Disease (also called Hexosaminidase deficiency)

B1 Question 1 Foundation

Cystic Fibrosis Carrier Testing

Two copies of each autosomal gene affect phenotype.

Friday, January 4. Bell Work:

What You ll Learn. Genetics Since Mendel. ! Explain how traits are inherited by incomplete dominance

The Cystic Fibrosis Gene. about. CF is one of the most common genetic diseases that cause death in both children and

Cystic Fibrosis. Information for Caregivers

p and q can be thought of as probabilities of selecting the given alleles by

- Aya Alomoush. - Talal Al-Zabin. - Belal Azab. 1 P a g e

Genetic Diseases. SCPA202: Basic Pathology

PULMONARY SURFACTANT, ALPHA 1 ANTITRYPSIN INHIBITOR DEFICIENCY, AND CYSTIC FIBROSIS DR. NABIL BASHIR BIOCHEMISTRY/RESPIRATORY SYSTEM

TEST INFORMATION Test: CarrierMap GEN (Genotyping) Panel: CarrierMap Expanded Diseases Tested: 311 Genes Tested: 299 Mutations Tested: 2647

NOTES: : HUMAN HEREDITY

BIO113 Exam 2 Ch 4, 10, 13

Figure 1: Transmission of Wing Shape & Body Color Alleles: F0 Mating. Figure 1.1: Transmission of Wing Shape & Body Color Alleles: Expected F1 Outcome

Recessive Genetic Disorders! A recessive trait is expressed when the individual is homozygous recessive for the trait.

Case Study What is the Relationship Between the Cell Membrane and Cystic Fibrosis?

Hths 2231 Laboratory 3 Genetics

The basic methods for studying human genetics are OBSERVATIONAL, not EXPERIMENTAL.

Genetic Disorders. PART ONE: Detecting Genetic Disorders. Amniocentesis Chorionic villus sampling Karyotype Triple Screen Blood Test

Pedigree Analysis. Genetic disorders. Dominant inheritance. Recessive inheritance. Autosomal vs. sex-linked traits. X-linked recessive inheritance

Genetic diseases. - chromosomal disorders (aneuploidy) - mitochondrial inherited diseases (female lineage transmission)

Cystic Fibrosis in Canada

"Management and Treatment of Patients with Cystic fibrosis (CF)

Genome - Wide Linkage Mapping

THE ROLE OF CFTR MUTATIONS IN CAUSING CYSTIC FIBROSIS (CF)

Lecture 17: Human Genetics. I. Types of Genetic Disorders. A. Single gene disorders

Genetic Counseling PSI AP Biology

Pedigree Analysis Why do Pedigrees? Goals of Pedigree Analysis Basic Symbols More Symbols Y-Linked Inheritance

FAMILY PLANNING DOESN T HAVE TO BE ONE OF THEM

UNDERSTANDING CYSTIC FIBROSIS

MENDELIAN GENETICS IN HUMANS

Essential Questions. Basic Patterns of Human Inheritance. Copyright McGraw-Hill Education

Complications in single gene analysis

What is Cystic Fibrosis? CYSTIC FIBROSIS. Genetics of CF

Problem set questions from Final Exam Human Genetics, Nondisjunction, and Cancer

Lesson Overview Human Chromosomes

A Case of Cystic Fibrosis

Goals Basic defect Pathophysiology Clinical i l signs and symptoms Therapy

Evolu&on of Disease genes

RAZAN AL-ZOUBI. Farah Albustanji BELAL AZAB. 1 P a g e

E-BOOK # PANCREATIC ENZYMES FOR CYSTIC FIBROSIS ARCHIVE

Cystic Fibrosis. Kevin Imah - Disorder Specialist Ph.D Vanessa Godinez - Genetic Counselor M.D. Study: Samuel Elliott - Parent & Patient

Cystic Fibrosis New Patient Binder Cystic Fibrosis Center Pediatric Pulmonary Division

Evolu+on of Disease genes

Bio 100 Guide 08.

Medical Policy An independent licensee of the Blue Cross Blue Shield Association

Basic Patterns of Human Inheritance. Reading Preview. Recessive Genetic Disorders. Essential Questions

Guided Notes: Simple Genetics

CYSTIC FIBROSIS OBJECTIVES NO CONFLICT OF INTEREST TO DISCLOSE

Patterns in Inheritance. Chapter 10

Pedigree Construction Notes

QUESTIONSHEET 1. (b)name two specific types of gene mutation and give two examples of gene mutation.

Cystic Fibrosis Foundation Patient Registry 2013

Unit 3: DNA and Genetics Module 9: Human Genetics

Human Genetic Mutations

A review of Cystic Fibrosis

GENETIC TESTING: IN WHOM AND WHEN

Patterns of Inheritance

Human Genetics Notes:

Bio 105 Guide 08.

Chapter 4 PEDIGREE ANALYSIS IN HUMAN GENETICS

Patterns of Inheritance

Biology 12. Mendelian Genetics

Mendel. The pea plant was ideal to work with and Mendel s results were so accurate because: 1) Many. Purple versus flowers, yellow versus seeds, etc.

Human Inheritance. Use Target Reading Skills. Patterns of Human Inheritance. Modern Genetics Guided Reading and Study

Psych 3102 Lecture 3. Mendelian Genetics

Compound heterozygosity Yurii S. Aulchenko yurii [dot] aulchenko [at] gmail [dot] com. Thursday, April 11, 13

Genetics Unit Exam. Number of progeny with following phenotype Experiment Red White #1: Fish 2 (red) with Fish 3 (red) 100 0

Single Gene (Monogenic) Disorders. Mendelian Inheritance: Definitions. Mendelian Inheritance: Definitions

Agro/Ansc/Bio/Gene/Hort 305 Fall, 2017 MEDICAL GENETICS AND CANCER Chpt 24, Genetics by Brooker (lecture outline) #17

Lab Activity 36. Principles of Heredity. Portland Community College BI 233

Mendelian Inheritance. Jurg Ott Columbia and Rockefeller Universities New York

CYSTIC FIBROSIS Risk Factors Epidemiology Pathogenesis Defective protein synthesis (10%) Abnormal protein folding, processing & trafficking

Mendelian Genetics and Beyond Chapter 4 Study Prompts

EEB 122b FIRST MIDTERM

(b) What is the allele frequency of the b allele in the new merged population on the island?

Questions Q1. ) in the box next to your answer. (1) A FF B Ff C ff. D ff (ii) Explain why a person with cystic fibrosis (CF) may lose body mass.

Transcription:

Module I: Introduction to the disease Give a brief introduction to the disease, considering the following: the symptoms that define the syndrome, the range of phenotypes exhibited by individuals with the disorder, whether environment plays a role in the severity of the disease, the physiological and psychological effects of having the disorder, and the prognosis and quality of life. What is the epidemiology of the disease? That is, how often does the disease occur, in how many births? Is there higher incidence in certain populations or geographical areas? If so, what explanations have been proposed? Briefly discuss the history of the disease. Who discovered it and when? How has understanding of the disease changed over time? What issues concern advocacy groups for the disorder (e.g., legal, ethical, social, financial)? What is the inheritance pattern (e.g., autosomal, sex-linked, dominant, recessive, etc.)? Define the genetic cause of the disease. What gene(s) are affected? What is the locus on the human genome? Briefly describe the wild-type function of the gene product. What types of mutations most commonly lead to the disease? How do these mutations arise? Sixty-Five Roses 1

Cystic Fibrosis: Summary Give a brief introduction to the disease, considering the following: the symptoms that define the syndrome, the range of phenotypes exhibited by individuals with the disorder, whether environment plays a role in the severity of the disease, the physiological and psychological effects of having the disorder, and the prognosis and quality of life. Body produces thick mucus due to a malfunction in the Na and chloride channels Symptoms: Salty skin Coughing Pneumonia Excessive Appetite Failure to Thrive http://health.allrefer.com/ Cystic Fibrosis: Range Give a brief introduction to the disease, considering the following: the symptoms that define the syndrome, the range of phenotypes exhibited by individuals with the disorder, whether environment plays a role in the severity of the disease, the physiological and psychological effects of having the disorder, and the prognosis and quality of life. Symptoms can vary in severity, though all patients progressively worsen 15-20% of CF newborns have an obstructed intestine and need surgery Clubbing of the fingers and toes can result from low blood O 2 levels Males are generally infertile (90%), while females can sometimes conceive Environment has little affect on severity http://health.allrefer.com/ 2

Cystic Fibrosis: Effects Give a brief summary of the disease, considering the following: the symptoms that define the syndrome, the range of phenotypes exhibited by individuals with the disorder, the physiological and psychological effects of having the disorder, and the prognosis and quality of life for individuals with the disorder. Afflicted individuals cannot maintain physical activity Therapies are difficult and timeconsuming, and most treat only symptoms Secondary lung infection is common Diets must be enriched to compensate for nutrient malabsorption Source -- Cystic Fibrosis Foundation: www.cff.org/facts.htm Back drumming to loosen mucus is a common CF therapy Cystic Fibrosis: Prognosis Give a brief summary of the disease, considering the following: the symptoms that define the syndrome, the range of phenotypes exhibited by individuals with the disorder, the physiological and psychological effects of having the disorder, and the prognosis and quality of life for individuals with the disorder. There is no cure Quality of life deteriorates with time Modern treatment has increased survival, but only 1/2 of CF patients will live beyond 30 years Back drumming to loosen mucus is a common CF therapy 3

Cystic Fibrosis: History Briefly discuss the history of the disease. Who discovered it and when? How has understanding of the disease changed over time? What issues concern advocacy groups for the disorder (e.g., legal, ethical, social, financial)? 1955: Cystic Fibrosis Foundation 1990: Gene therapy in vitro 1938: Dorothy Anderson 1989: CF gene discovered Better understanding has led to more effective treatment of symptoms Newborns may be treated with surgery to clear an obstructed intestine. Enriched diet compensates for nutrient malabsorption. Antibiotics treat lung infections. Median life expectancy was less than a year in 1940, and is now over 30 years. Sources: www.cff.org/facts.htm Cystic Fibrosis Foundation Welsh, M.J., and Smith, A.E. Cystic Fibrosis. Scientific American (Dec. 1995):52-59. Cystic Fibrosis: Epidemiology What is the epidemiology of the disease? That is, how often does the disease occur, in how many births? Is there higher incidence in certain populations or geographical areas? If so, what explanations have been proposed? Most common fatal hereditary disease in the US and much of Europe 30,000 people in the US have CF 1 of 25 Caucasians is a carrier, and 1/2400 individuals are affected Frequencies are lowest in Asian populations, with only 1/150 being carriers and 1/89,000 http://www3.nbnet.nb.ca/normap/cf.htm http://www.uihealthcare.com/ http://www.cincinnatichildrens.org 4

Cystic Fibrosis: Advocacy Briefly discuss the history of the disease. Who discovered it and when? How has understanding of the disease changed over time? What issues concern advocacy groups for the disorder (e.g., legal, ethical, social, financial)? Advocacy and research groups are common world-wide Groups provide education and support networks, sponsoring local community events Research funding aims to provide better treatments and create greater quality of living Cystic Fibrosis: Inheritance What is the inheritance pattern (e.g., autosomal, sex-linked, dominant, recessive, etc.)? Autosomal Recessive Trait Simple Mendelian Inheritance 5

Cystic Fibrosis: Gene Define the genetic cause of the disease. What gene(s) are affected? What is the locus on the human genome? Briefly describe the wild-type function of the gene product. What types of mutations most commonly lead to the disease? How do these mutations arise? CFTR is the Cystic Fibrosis Transmembrane Conductance Regulator Mutations in this gene cause CF Found in 1989 Locus: 7q31.2 (long arm of chromosome 7, band 31, subband 2) Source: OMIM, NCBI MapViewer, and Entrez Gene Cystic Fibrosis: Gene Function Define the genetic cause of the disease. What gene(s) are affected? What is the locus on the human genome? Briefly describe the wild-type function of the gene product. What types of mutations most commonly lead to the disease? How do these mutations arise? CFTR codes for a transmembrane protein that functions in transporting chloride ions in and out of cells Lack of CFTR causes excess mucus secretion 6

Cystic Fibrosis: Mutations Define the genetic cause of the disease. What gene(s) are affected? What is the locus on the human genome? Briefly describe the wild-type function of the gene product. What types of mutations most commonly lead to the disease? How do these mutations arise? Deletion of codon 508 (TTT--phenylalanine) ΔF508 Accounts for 70% of mutations in CF patients 700 reported mutations 12 other mutations account for 15% Remaining 15% much less frequent Because the disorder is recessive, most mutations are inherited. Source: OMIM, http://homepages.strath.ac.uk/~dfs99109/bb310/mglect7.html CF: Heterozygous Advantage? What is the epidemiology of the disease? That is, how often does the disease occur, in how many births? Is there higher incidence in certain populations or geographical areas? If so, what explanations have been proposed? Cystic fibrosis is surprisingly common in Caucasians (1/25 are carriers) The mutated CF gene may be advantageous to the heterozygote. Salmonella typhi, which causes typhoid fever, uses CFTR for entry into epithelial cells. Heterozygous delta- F508 Cftr mice internalized 86% fewer S. typhi than did wildtype mice. Source: OMIM, Pier, G. B., et al.: Nature 393: 79-82, 1998. 7

CF: Heterozygote Advantage? What is the epidemiology of the disease? That is, how often does the disease occur, in how many births? Is there higher incidence in certain populations or geographical areas? If so, what explanations have been proposed? Cholera and pathogens that cause chloride ionsecreting diarrheas also use CFTR as a gate into the cells. But diarrhea-causing pathogens are found all over the world--why were mutations only preserved in N. Europe? Mutant alleles lead to chronic excessive salt loss--a major disadvantage in hot climates? Source: http://www.people.virginia.edu/~rjh9u/cysfib.html CF: Take Home Message 1. Cystic Fibrosis results in thick mucus buildup due to faulty salt transport, leading to respiratory and digestive problems 2. Many populations are affected but it is most common in Caucasians of European descent 3. CF Is inherited in an autosomal recessive pattern 4. CF is caused by defects in the CFTR gene 5. Deletion of phenylalanine 508 accounts for 70% of mutations. 6. Heterozygotes may be more resistant to Typhoid fever, Cholera, and chloride ion-secreting diarrheas. 8