Biology (MindTap Course List)
11th Edition
ISBN: 9781337392938
Author: Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 16.3, Problem 7LO
State whether each of the following genetic defects is inherited as an autosomal recessive, autosomal dominant, or X-linked recessive trait: phenylketonuria (PKU), sickle cell anemia, cystic fibrosis, Tay-Sachs disease, Huntington’s disease, and hemophilia A.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Genetic disorders
Complete the following statements to describe several genetic disorders and their symptoms. Choices can be used more than once.
The
disorder called
causes blue-colored skin,
sickle-cell disease
osteogenesis imperfecta
The
disorder called
that leads to weakened, brittle bones.
causes defective collagen
methemoglobinemia
autosomal dominant
The
disorder called
causes abnormally thick
mucus in the bronchial tubes and pancreatic ducts.
autosomal recessive
The
disorder called
leads to progressive
cystic fibrosis
degeneration of neurons in the brain.
alkaptonuria
The
disorder called
causes urine to be black.
Huntington disease
acer
%23
24
&
4
8.
9.
e
y
u
< 6
3) State whether each of the following genetic defects is inherited as an autosomal recessive, autosomal dominant, or X-linked recessive trait: phenylketonuria (PKU), sickle cell anemia, cystic fibrosis, Tay-Sachs disease, Huntington’s disease, and hemophilia A.
Describe in words the likely transmission of an autosomal dominant disorder. Include details of the parent’s genotype and subsequent pattern and probability of inheritance of the single gene disorder for the offspring produced and provide an example of an autosomal dominant disorder
Chapter 16 Solutions
Biology (MindTap Course List)
Ch. 16.1 - Distinguish between karyotyping and pedigree...Ch. 16.1 - Prob. 2LOCh. 16.1 - Prob. 3LOCh. 16.1 - Prob. 1CCh. 16.1 - Prob. 2CCh. 16.1 - Describe two ways in which genome database...Ch. 16.1 - Prob. 4CCh. 16.2 - Explain how nondisjunction in meiosis is...Ch. 16.2 - Distinguish among the following structural...Ch. 16.2 - Prob. 6LO
Ch. 16.2 - VISUALIZE Draw a simple sketch illustrating how...Ch. 16.2 - Prob. 2CCh. 16.2 - Prob. 3CCh. 16.2 - Prob. 4CCh. 16.3 - State whether each of the following genetic...Ch. 16.3 - Which of the following genetic diseases is/are...Ch. 16.3 - Prob. 2CCh. 16.3 - Prob. 3CCh. 16.4 - Briefly discuss the process of gene therapy,...Ch. 16.4 - Prob. 1CCh. 16.5 - State the relative advantages and disadvantages of...Ch. 16.5 - Distinguish between genetic screening programs for...Ch. 16.5 - Prob. 1CCh. 16.5 - Prob. 2CCh. 16.6 - Prob. 11LOCh. 16.6 - Prob. 1CCh. 16.6 - CONNECT To be expressed, an autosomal recessive...Ch. 16.6 - Prob. 3CCh. 16 - Prob. 1TYUCh. 16 - An abnormality in which there is one more or one...Ch. 16 - The failure of chromosomes to separate normally...Ch. 16 - Prob. 4TYUCh. 16 - Prob. 5TYUCh. 16 - Prob. 6TYUCh. 16 - Prob. 7TYUCh. 16 - Prob. 8TYUCh. 16 - Examine the following pedigrees. Which is the most...Ch. 16 - Examine the following pedigrees. Which is the most...Ch. 16 - Prob. 11TYUCh. 16 - SCIENCE, TECHNOLOGY, AND SOCIETY Imagine that you...Ch. 16 - A common belief about human genetics is that an...Ch. 16 - Prob. 14TYUCh. 16 - EVOLUTION LINK Explain some of the evolutionary...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Mention any two autosomal genetic disorders with their symptoms.arrow_forwardWhat are the odds of the person with sickle cell anemia disorder passing it on to their children if the other person is homozygous dominant, heterozygous, or homozygous recessive for the trait?arrow_forwardIn Ingested poisoning and carbon monoxide poisoning, are there any measures that could prevent this form occuring? Is this disease/disorder or medical emergency precentable? Or is there a way to lessen your chances of getting this disease/disorder? (if it's a genetic disease the answer is likely no) How?arrow_forward
- On the basis of the information provided, is the inheritance of haemophilia: autosomal or sex-linked? dominant or recessivearrow_forwardReview the process of autosomal dominant inheritance by coloring the following figures. In this instance the father is affected in the mother is unaffected to illustrate the transmission of the disorder from the father to the children color the figures as described.arrow_forwardWhich of the following genetic diseases is/are inherited as an autosomal dominant trait: sickle cell anemia, hemophilia A, Huntington’s disease?arrow_forward
- Please help me with the following question: Von Willebrand disease is an inherited bleeding disorder. People with von Willebrand disease take a much longer period for blood to clot/stop than others. von Willebrand disease is either inherited in an autosomal dominant pattern or in an autosomal recessive pattern. Question: what is the genotype of the disorder? what are the phenotypic effects of the disorder? What is happening with the DNA to cause the phenotypic effects?arrow_forwardDescribe and discuss the genetics of the following inherited disorders:A. Cystic FibrosisB. Sickle cell diseaseC. AchondroplasiaD. Huntington’s diseasearrow_forwardDescribe the individuals with the following chromosomal abnormalities: Trisomy at chromosome 21 XXY XOarrow_forward
- Explain how various genetic disorders can occur.arrow_forwardTell me whether it is autosomal reccessive inheritance,autosomal domiant inheritance,sex-linked reccessive inheritance, sex-linked dominay inheritance or y-linked inheritance.arrow_forwardWhat is genetic disorders? Explain by giving an example.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Biology (MindTap Course List)BiologyISBN:9781337392938Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. BergPublisher:Cengage Learning
Medical Terminology for Health Professions, Spira...Health & NutritionISBN:9781305634350Author:Ann Ehrlich, Carol L. Schroeder, Laura Ehrlich, Katrina A. SchroederPublisher:Cengage Learning
Biology (MindTap Course List)
Biology
ISBN:9781337392938
Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher:Cengage Learning
Medical Terminology for Health Professions, Spira...
Health & Nutrition
ISBN:9781305634350
Author:Ann Ehrlich, Carol L. Schroeder, Laura Ehrlich, Katrina A. Schroeder
Publisher:Cengage Learning
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY