A homozygous mother has retinoblastoma, a dominant sex-linked disorder carried on the X chromosome. The father does not have this disorder. What is the chance they will have a child with this disorder? 1) 0% 2) 25% 3) 50% 4) 75% 5) 100%

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
icon
Related questions
Topic Video
Question
### Inheritance of Retinoblastoma (Dominant X-linked Disorder)

**Question:**
A homozygous mother has retinoblastoma, a dominant sex-linked disorder carried on the X chromosome. The father does not have this disorder. What is the chance they will have a child with this disorder?

**Options:**
1. 0%
2. 25%
3. 50% **(Selected Answer)**
4. 75%
5. 100%

#### Explanation:

Retinoblastoma is a condition that is passed on through the X chromosome. Since it is a dominant disorder, only one copy of the defective gene is needed for an individual to exhibit the disorder.

Given that the mother is homozygous for the disorder, she carries two copies of the defective gene (X^R X^R). The father does not have the disorder and therefore carries the normal gene on his X chromosome (X^r Y).

During reproduction, the mother can only pass on the defective X chromosome to her children (X^R), while the father can pass either his normal X chromosome (X^r) to daughters or his Y chromosome (Y) to sons.

- **Daughters (XX):**
  - Inherit X^R from mother (always)
  - Inherit X^r from father (always)

  Outcome: X^R X^r → All daughters will have retinoblastoma.

- **Sons (XY):**
  - Inherit X^R from mother (always)
  - Inherit Y from father (always)

  Outcome: X^R Y → All sons will have retinoblastoma.

Therefore, regardless of the gender of the child, each child has a 100% chance of inheriting the disorder.

Making an educated guess from the given options, although 100% would be the correct answer in a detailed genetic explanation, the text provides "50%" (option 3) as the selected answer which may indicate incomplete understanding or an error in the given options. Depending on the educational level, further review might be needed for accuracy.
Transcribed Image Text:### Inheritance of Retinoblastoma (Dominant X-linked Disorder) **Question:** A homozygous mother has retinoblastoma, a dominant sex-linked disorder carried on the X chromosome. The father does not have this disorder. What is the chance they will have a child with this disorder? **Options:** 1. 0% 2. 25% 3. 50% **(Selected Answer)** 4. 75% 5. 100% #### Explanation: Retinoblastoma is a condition that is passed on through the X chromosome. Since it is a dominant disorder, only one copy of the defective gene is needed for an individual to exhibit the disorder. Given that the mother is homozygous for the disorder, she carries two copies of the defective gene (X^R X^R). The father does not have the disorder and therefore carries the normal gene on his X chromosome (X^r Y). During reproduction, the mother can only pass on the defective X chromosome to her children (X^R), while the father can pass either his normal X chromosome (X^r) to daughters or his Y chromosome (Y) to sons. - **Daughters (XX):** - Inherit X^R from mother (always) - Inherit X^r from father (always) Outcome: X^R X^r → All daughters will have retinoblastoma. - **Sons (XY):** - Inherit X^R from mother (always) - Inherit Y from father (always) Outcome: X^R Y → All sons will have retinoblastoma. Therefore, regardless of the gender of the child, each child has a 100% chance of inheriting the disorder. Making an educated guess from the given options, although 100% would be the correct answer in a detailed genetic explanation, the text provides "50%" (option 3) as the selected answer which may indicate incomplete understanding or an error in the given options. Depending on the educational level, further review might be needed for accuracy.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps

Blurred answer
Knowledge Booster
Mitochondrial mutations
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
Recommended textbooks for you
Human Anatomy & Physiology (11th Edition)
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:
9780134580999
Author:
Elaine N. Marieb, Katja N. Hoehn
Publisher:
PEARSON
Biology 2e
Biology 2e
Biology
ISBN:
9781947172517
Author:
Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:
OpenStax
Anatomy & Physiology
Anatomy & Physiology
Biology
ISBN:
9781259398629
Author:
McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:
Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:
9780815344322
Author:
Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:
W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:
9781260159363
Author:
Martin, Terry R., Prentice-craver, Cynthia
Publisher:
McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Inquiry Into Life (16th Edition)
Biology
ISBN:
9781260231700
Author:
Sylvia S. Mader, Michael Windelspecht
Publisher:
McGraw Hill Education