Which of the following is not an aneuploid condition? a. Turner syndrome c. Alagille sy

Name: Problem 18, Chapter 10: Biology
Uploaded: 2021-01-05T19:27:04-08:00
Duration: 2 min 56 s
Channel: Bryan Lynn
Description: Which of the following is not an aneuploid condition? a. Turner syndrome c. Alagille syndrome b. Down syndrome d. Klinefelter syndrome

step 1 And in particular, we're looking at a new ploidy. So what does that mean? That means to have an

Question

Which of the following is not an aneuploid condition? $$\begin{array}{ll}{\text { a. Turner syndrome }} & {\text { c. Alagille syndrome }} \\ {\text { b. Down syndrome }} & {\text { d. Klinefelter syndrome }}\end{array}$$

   Which of the following is not an aneuploid condition?
$$\begin{array}{ll}{\text { a. Turner syndrome }} & {\text { c. Alagille syndrome }} \\ {\text { b. Down syndrome }} & {\text { d. Klinefelter syndrome }}\end{array}$$

Biology

Sylvia S. Mader,… 12th Edition

Chapter 10, Problem 18

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Solved by Expert Bryan Lynn

01/05/2021

Step 1

Aneuploidy refers to a condition where there is an abnormal number of chromosomes. This could mean having an extra chromosome or missing one. Show more…

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Which of the following is not an aneuploid condition? $$\begin{array}{ll}{\text { a. Turner syndrome }} & {\text { c. Alagille syndrome }} \\ {\text { b. Down syndrome }} & {\text { d. Klinefelter syndrome }}\end{array}$$

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Key Concepts

Aneuploidy

Aneuploidy refers to the presence of an abnormal number of chromosomes in a cell, a state that typically arises from errors in cell division such as nondisjunction. This condition leads to imbalances in gene dosage, which in turn can cause various developmental and physical abnormalities. It is a key concept in understanding several chromosomal disorders where the number of chromosomes deviates from the normal complement.

Mutation-Based Genetic Disorders

Not all genetic disorders are caused by abnormal chromosome numbers; some result from mutations within a gene. These single-gene or mutation-based disorders occur due to changes such as point mutations, deletions, or insertions that alter a gene’s function, without affecting the overall chromosomal count. This distinction is important in genetics to differentiate conditions arising from numerical chromosomal errors from those due to specific gene mutations.

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