Anatomy & Physiology
1st Edition
ISBN: 9781938168130
Author: Kelly A. Young, James A. Wise, Peter DeSaix, Dean H. Kruse, Brandon Poe, Eddie Johnson, Jody E. Johnson, Oksana Korol, J. Gordon Betts, Mark Womble
Publisher: OpenStax College
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Textbook Question
Chapter 28, Problem 28RQ
Marfan syndrome is inherited in an autosomal dominant pattern. Which of the following is true?
- Female offspring are more Likely to be carriers of the disease.
- Male offspring are more likely to inherit the disease.
- Male and female offspring have the same likelihood of inheriting the disease.
- Female offspring are more likely to inherit the disease.
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In 1-3 sentences define the following heredity types:
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Hemophilia is due to a sex-linked gene. It is recessive and found on the X chromosome. A woman who is a carrier for hemophilia marries a normal man. What will be the possible phenotypes of their children? (use the letter “H”)
Chapter 28 Solutions
Anatomy & Physiology
Ch. 28 - View this time-lapse movie...Ch. 28 - Visit this site...Ch. 28 - Sperm and ova are similar in terms of ________....Ch. 28 - Although the male ejaculate contains hundreds of...Ch. 28 - As sperm first reach the oocyte, they will contact...Ch. 28 - Fusion of pronuclei occurs during ________....Ch. 28 - Sperm must first complete ________ to enable the...Ch. 28 - Cleavage produces daughter cells called ________....Ch. 28 - The conceptus, upon reaching the uterus, first...Ch. 28 - The inner cell mass of the blastocyst is destined...
Ch. 28 - Which primary germ layer gave rise to the cells...Ch. 28 - What would happen if the trophoblast did not...Ch. 28 - During what process does the amnion envelop the...Ch. 28 - The placenta is formed from ________. the embryos...Ch. 28 - The foramen ovale causes the fetal circulatory...Ch. 28 - What happens to the urine excreted by the fetus...Ch. 28 - During weeks 9–12 of fetal development,...Ch. 28 - Progesterone secreted by the placenta suppresses...Ch. 28 - Which of the following is a possible culprit of...Ch. 28 - How does the decrease in progesterone at the last...Ch. 28 - Which of these fetal presentations is the easiest...Ch. 28 - Which of these shunts exists between the right and...Ch. 28 - Why is brown fat important? It is the newborns...Ch. 28 - Constriction of umbilical blood vessels during...Ch. 28 - Alveoli are connected to the lactiferous sinuses...Ch. 28 - How is colostrum most important to a newborn? It...Ch. 28 - Mature breast milk ________. has more sodium than...Ch. 28 - Marfan syndrome is inherited in an autosomal...Ch. 28 - In addition to codominance, the ABO blood group...Ch. 28 - Zoe has cystic fibrosis. Which of the following is...Ch. 28 - Darcy and Raul are having difficulty conceiving a...Ch. 28 - Sherrise is a sexually active college student. On...Ch. 28 - Approximately 3 weeks after her last menstrual...Ch. 28 - The Food and Nutrition Board of the Institute of...Ch. 28 - What is the physiological benefit of incorporating...Ch. 28 - Why would a premature infant requite supplemental...Ch. 28 - Devin is 35 weeks pregnant with her first child...Ch. 28 - Janine is 41 weeks pregnant with her first child...Ch. 28 - Describe how the newborns fust breath alters the...Ch. 28 - Newborns are at much higher risk for dehydration...Ch. 28 - Describe the transit of breast milk from...Ch. 28 - A woman who stopped breastfeeding suddenly is...Ch. 28 - Explain why it was essential that Mendel perform...Ch. 28 - How can a female carrier of an X-linked recessive...
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- Assume for a moment that a child has a autosomal recessive disorder, but both parents appear normal. What is the genotype of both parents? : one parent must be homozygous dominant : both parents must be homozygous recessive : both parents are heterozygous : both parents nust be homozygous dominantarrow_forwardBecause Elsa has received a confirmed diagnosis of beta-thalassemia major, which of the following statements is true about her parents? Only her mother carried the gene that caused her blood disorder. Only her father carried the gene that caused her blood disorder. If her parents have another child naturally, there is a 100% chance that the second child will be diagnosed with beta-thalassemia major. If her parents have another child naturally, there is a 25% chance that the second child will be diagnosed with beta-thalassemia major.arrow_forwardTongue rolling is an autosomal dominant trait. What would be the phenotype of a person who is heterozygous for this trait?arrow_forward
- Hereditary hemochromatosis is an autosomal recessive genetic disorder that causes the body to absorb too much iron from the diet. This excess iron is stored in the body's tissues and organs, particularly the skin, heart, liver, pancreas, and joints. Because humans cannot increase the excretion of iron, excess iron can overload and eventually damage tissues and organs. A man who had hemophilia (an X-linked recessive genetic disorder), married a woman who had no family history of hemophilia whatsoever. The couple had consulted a genetic counselor when they first contemplated having children due to concerns that their future children might have hemophilia. Genetic testing of both future parents revealed that the husband did, in fact, possess the Hemophilia A allele but his wife was completely normal with respect to hemophilia. Much to their shock, their first child, a daughter, had a mild blood clotting disorder. Karyotyping was performed to determine whether this daughter had an…arrow_forwardMention any two autosomal genetic disorders with their symptoms.arrow_forwardA woman homozygous for normal height, with freckles, almond-shaped eyes, small nose, and Type A blood, has a Type O mother with no freckles and a type AB father with round eyes. She is engaged to a man with achondroplasia, round eyes and medium sized nose. Unlike his father, hismother is of normal height. Both his parents have Type O blood but nobody from both sides of his family has or had freckles. a. Write the COMPLETE genotypes of the man and the woman. Clearly indicate which genotype belongs to whom. b. Based on their genotypes, what is the probability that they will have: b.1 a child with Achondroplasia? b.2 a child of normal height? b.3 a child with type AB blood? b.4 a daughter with round eyes, freckles, and medium sized nose? b.5 a son with almond eyes, no freckles, and small nose?b.6 a daughter with same genotype as the woman? b.7 a son with same genotype as the man?arrow_forward
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