Cell Biology: Heteroploidy Quiz

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Questions and Answers

What is Turner syndrome also known as?

  • Gonadal dysgenesis (correct)
  • Klinefelter syndrome
  • Down syndrome
  • Marfan syndrome

Turner syndrome is caused by what chromosomal condition?

  • Trisomy of the X chromosome
  • Monosomy of the X chromosome (correct)
  • Duplication of chromosome 21
  • Deletion of a segment of chromosome 5

How frequently does Turner syndrome occur in female newborns?

  • 1 in 100 – 1 in 500
  • 1 in 2000 – 1 in 3000 (correct)
  • 1 in 500 – 1 in 1000
  • 1 in 4000 – 1 in 6000

What percentage of fetuses with Turner syndrome are spontaneously aborted during the first trimester of pregnancy?

<p>About 99% (C)</p> Signup and view all the answers

What is XXX syndrome also known as?

<p>Triplo-X syndrome &amp; trisomy X (D)</p> Signup and view all the answers

XXX syndrome occurs exclusively in which gender and how frequently?

<p>Females ONLY, about once in every 1,000 female births (B)</p> Signup and view all the answers

What is Heteroploidy in cell biology?

<p>An abnormal chromosome number in cells (B)</p> Signup and view all the answers

What is the primary cause of Heteroploidy?

<p>Irregular mitosis (D)</p> Signup and view all the answers

In which type of cells is Heteroploidy most often observed?

<p>Cancer cells (B)</p> Signup and view all the answers

What causes Cri du chat syndrome?

<p>Deletion of part of the short arm of chromosome 5 (D)</p> Signup and view all the answers

What is the incidence rate of Cri du chat syndrome?

<p>1 in 37,000 to 50,000 live births (A)</p> Signup and view all the answers

In terms of gender, how does Cri du chat syndrome predominantly occur?

<p>More common in females (B)</p> Signup and view all the answers

What is the karyotype of a person with Klinefelter syndrome?

<p>47,XXY (B)</p> Signup and view all the answers

Which syndrome is caused by the deletion of a segment of chromosome 5?

<p>Turner syndrome (B)</p> Signup and view all the answers

What is the primary cause of Down syndrome?

<p>Duplication of chromosome 21 (C)</p> Signup and view all the answers

What is the primary cause of Turner syndrome?

<p>Deletion of part of the X chromosome (A)</p> Signup and view all the answers

What does 'Haploidy' refer to in cell biology?

<p>A normal chromosome number in cells (C)</p> Signup and view all the answers

Where is Heteroploidy most often observed?

<p>Cancer cells (D)</p> Signup and view all the answers

What causes Down syndrome?

<p>Mutation in chromosome 21 (D)</p> Signup and view all the answers

What is the incidence rate of Turner syndrome?

<p>1 in 100,000 to 120,000 live births (D)</p> Signup and view all the answers

In terms of gender, how does Turner syndrome predominantly occur?

<p>More common in females (A)</p> Signup and view all the answers

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Study Notes

Chromosomal Conditions

  • Turner syndrome is also known as 45,X or 45,X0.
  • Turner syndrome is caused by a chromosomal condition where one of the sex chromosomes is missing or partially deleted.

Incidence Rate of Turner Syndrome

  • Turner syndrome occurs in approximately 1 in 2,500 to 1 in 5,000 female newborns.

Spontaneous Abortions

  • Approximately 99% of fetuses with Turner syndrome are spontaneously aborted during the first trimester of pregnancy.

XXX Syndrome

  • XXX syndrome is also known as Triplo-X syndrome.
  • XXX syndrome occurs exclusively in females and affects approximately 1 in 1,000 females.

Heteroploidy

  • Heteroploidy refers to a condition in cell biology where a cell contains multiple sets of chromosomes.
  • The primary cause of Heteroploidy is chromosomal duplication or deletion.
  • Heteroploidy is most often observed in cancer cells.

Cri du Chat Syndrome

  • Cri du chat syndrome is caused by the deletion of a segment of chromosome 5.
  • The incidence rate of Cri du chat syndrome is approximately 1 in 20,000 to 1 in 50,000 births.
  • Cri du chat syndrome predominantly occurs in females.

Klinefelter Syndrome

  • The karyotype of a person with Klinefelter syndrome is 47,XXY.

Down Syndrome

  • The primary cause of Down syndrome is the presence of an extra copy of chromosome 21 (trisomy 21).

Turner Syndrome

  • The primary cause of Turner syndrome is the loss or deletion of a sex chromosome.

Haploidy

  • 'Haploidy' refers to a cell with a single set of chromosomes.

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