Answered: Which of the following disorders in…

Which of the following disorders in humans has an X-linked recessive inheritance pattern? Red-green color blindness Marfan syndrome Tay-Sachs disease Hutchinson-Gilford progeria

Human Biology (MindTap Course List)

11th Edition

ISBN:9781305112100

Author:Cecie Starr, Beverly McMillan

Publisher:Cecie Starr, Beverly McMillan

Chapter19: Introduction To Genetics

Section: Chapter Questions

Problem 9CT

See similar textbooks

Related questions

Q: PKU disease is recessive. A man and a woman are both carriers for PKU disease. Determine the…

A: KU disease is recessive. A man and a woman are both carriers of PKU disease. NormALLELE---------P;…

Q: II 4 5 II 1 2 3 4 5 6 7 IV 1 2 3 4 5 6 7 8 9

A: In the given pedigree, the trait skips generation, i.e., the trait appeared in the first generation…

Q: The pedigree shows inheritance of an autosomal recessive disease in an extended family. Assume…

A: Although the trait is skipped in the pedigree, autosomal recessive inheritance is discovered. The…

Q: How many Barr bodies in a person with genotype XXXXX? How is the structure of a Barr body different…

A: The mammalian males contain XY chromosome and females contain XX chromosome. So, the number of…

Q: Sickle cell anemia is inherited as an autosomal recessive condition. It also exhibits incomplete…

A: Sickle cell anemia (SCA) is a genetic disorder that occurs when an individual has two homozygous…

Q: What is the relationship between individual I-1 and individual III-2? Incidence of Hemophilia…

A: Introduction Haemophilia Is A Hereditary Condition That Affects The Body's Capacity To Form Blood…

Q: Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently…

A: Genetic disorders usually known to state Which passed down from one generation to the next. They may…

Q: The pedigree below shows a family affected by a disease. Assume that the individuals marked with an…

A: * Genotypes refers to genetic makeup of an organism which describes an organisms complete set of…

Q: The following X-linked recessive traits are found in fruit flies:vermilion eyes are recessive to red…

A: To calculate The map distance separating two genes

Concept explainers

Communication

Communication is a method of transferring information between two persons or organisms. Communication is possible using mutually understood behaviors such as signs, symbols, or language. In the year 1980, S. F. Scudder proposed communication theory. According to his ideas, all living beings on the earth communicate, but the methods of communication differ. Communication skills are now part of soft skills.

Question

Which of the following disorders in humans has an X-linked recessive inheritance pattern?

Red-green color blindness

Marfan syndrome

Tay-Sachs disease

Hutchinson-Gilford progeria

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

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

The young woman shown at right has albinismvery pale skin, white hair, and pale blue eyes. This phenotype is due to the absence of melanin, which imparts color to the skin, hair, and eyes. It typically is caused by a recessive allele. In the following situations, what are the probable genotypes of the father, the mother, and their children? a. Both parents have normal phenotypes; some of their children are albino and others are not. b. Both parents and all their children are albino. c. The mother is not albino, the father is albino, and one of their four children is albino.
Analysis of X-Linked Dominant and Recessive Traits A young boy is color-blind. His one brother and five sisters are not. The boy has three maternal uncles and four maternal aunts. None of his uncles children or grandchildren is color-blind. One of the maternal aunts married a color-blind man, and half of her children, both male and female, are color-blind. The other aunts married men who have normal color vision. All their daughters have normal vision, but half of their sons are color-blind. a. Which of the boys four grandparents transmitted the gene for color blindness? b. Are any of the boys aunts or uncles color-blind? c. Is either of the boys parents color-blind?
The pedigree below shows the inheritance of an autosomal recessive disorder in humans. Which of the following individuals is NOT known to be a carrier? I 1 2 II 1 2 3 4 III 1 2 5 O1-1 I-2 Il-1 Il-4 None of the above
Which of the following disorders in humans has an autosomal dominant inheritance pattern? Hemophilia Albinism Tay-Sachs disease Huntington’s disease
A man affected with Cacamania and a woman affected with Cacamania mate and have an unaffected daughter. Which of the following mechanisms of inheritance can not be ruled out? Choose all that can not be ruled out. Autosomal Recessive Autosomal Dominant Y-linked X-linked Recessive All of the mechanisms shown can be ruled out X-linked Dominant
The most common form of colorblindness is a recessive, sex-linked hereditary con dition caused by a defect on the X chromosome. Females are XX, while males are XY. Individuals inherit one chromosome from each parent, with equal probability; for example, an individual has a 50% chance of inheriting their father's X chromosome, and a 50% chance of inheriting their father's Y chromosome. If a male has an X chromosome with the defect, he is colorblind. However, a female with only one defective X chromo some will not be colorblind. Thus, colorblindness is more common in males than females; 7% of males are colorblind but only 0.5% of females are colorblind. (a) Assume that the X chromosome with the wild-type allele is X+ and the one with the disease allele is X. What is the expected frequency of each possible female genotype: X+X+, X+X¯, and X-X-? What is the expected frequency of each possible male genotype: X+ Y and X-Y? (b) Suppose that two parents are not colorblind. What is the…
An unaffected man and an unaffected woman mate and have a son affected with Kakamania. Which of the following mechanisms of inheritance can not be ruled out? Choose all that can not be ruled out. All of the mechanisms shown can be ruled out Y-linked X-linked Dominant Autosomal Recessive X-linked Recessive Autosomal Dominant
What describes a situation in which an allele's expression depends on the parent from which it was inherited? autosomal linkage chimerism genomic imprinting mosaicism
Red-green color blindness is inherited as an X-linked recessive (Xc). If a color-blind man marries a woman who is heterozygous for normal vision, what would be the expected phenotypes of their children with reference to this character? In your answer, specify in your phenotype descriptions the gender of the children. (For example, don’t just say 75% of the children would be colorblind – you would instead say 100 % of the daughters would be colorblind and 50% of the sons would be colorblind. Note that this is not a correct answer; it is just to give you an idea of how to explain the correct phenotypes of the cross.)___
People with trisomy 21 develop Down’s syndrome. What law of Mendelian inheritance is violated in this disease? What is the most likely way this occurs?
An unaffected man and an unaffected woman mate and have a daughter affected with Fifimania. Which of the following mechanisms of inheritance can not be ruled out? Choose all that can not be ruled out. Autosomal Recessive Autosomal Dominant X-linked Dominant X-linked Recessive All of the mechanisms shown can be ruled out Y-linked
For the following diseases with their potential pedigree, mode of inheritance and the responsible gene: (Pedigrees A, B, and C) -> Do Pedigree C Pedigree B, Autosomal dominant, Huntingtin gene Pedigree B, Autosomal dominant, CFTR gene Pedigree B, Autosomal dominant, HexA gene Pedigree B, Autosomal dominant, FGFR3 gene Pedigree A, Autosomal recessive, CFTR gene Pedigree A, Autosomal recessive, Beta-globin gene Pedigree A, Autosomal dominant, FGFR3 gene Pedigree B, X-linked dominant. Factor VIII gene Pedigree A, Autosomal dominant, Beta-globin gene Pedigree A. Autosomal recessive, Huntingtin gene Pedigree C, X-linked recessive, Factor VIII gene Pedigree A, Autosomal recessive, HexA gene