Cytogenetics

Descrição

Quiz sobre Cytogenetics, criado por rachelbird10 em 21-10-2015.
rachelbird10
Quiz por rachelbird10, atualizado more than 1 year ago
rachelbird10
Criado por rachelbird10 aproximadamente 9 anos atrás
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Resumo de Recurso

Questão 1

Questão
A structural chromosomal abnormality is described by which of the following?
Responda
  • Chromosome breakage with improper repair
  • Nondisjunction of chromosomes during Meiosis I
  • Nondisjunction of chromosomes during Meiosis II
  • Extra chromosomes created and added to genome

Questão 2

Questão
How many chromosomes could someone with polypoidy have?
Responda
  • 69 chromosomes
  • 47 chromosomes
  • 45 chromosomes

Questão 3

Questão
You can survive with only one X chromosome.
Responda
  • True
  • False

Questão 4

Questão
Dispermy results in?
Responda
  • Triploidy
  • Tetraploidy
  • Polyploidy

Questão 5

Questão
The most common pregnancy complication is [blank_start]spontaneous abortions[blank_end].
Responda
  • spontaneous abortions

Questão 6

Questão
A baby is born with feet shaped like rockers and clenched hands. The baby had poor prenatal growth. Which of the following describe the condition of the baby?
Responda
  • Edwards Syndrome, Nondisjunction
  • Edwards Syndrome, Robertsonian Translocation
  • Patau Syndrome, Nondisjuction
  • Patau Syndrome, Robertsonian Translocation

Questão 7

Questão
All of the following include trisomy. Down Syndrome is a defect in chromosome [blank_start]21[blank_end]. Edwards Syndrome is a defect in chromosome [blank_start]18[blank_end]. Patau is a defect in chromosome [blank_start]13[blank_end].
Responda
  • 13
  • 21
  • 18
  • 22
  • 19
  • 17
  • 15
  • 25

Questão 8

Questão
Turner Syndrome is a result of nondisjunction of maternal chromosomes.
Responda
  • True
  • False

Questão 9

Questão
The Turner Syndrome genotype is [blank_start]X[blank_end]. The Klinefelter genotype is [blank_start]XXY[blank_end]. The Tripe X Syndrome genotype is [blank_start]XXX[blank_end]. The last sex chromosome disorder involves paternal meiosis II nondisjunction and is called [blank_start]47, XYY[blank_end]
Responda
  • X
  • XXY
  • XXX
  • 47, XYY

Questão 10

Questão
Which of the following (more than one?) could be caused by maternal nondisjuction?
Responda
  • Turner Syndrome
  • Triple X Syndrome
  • Klinefelter Syndrome
  • Edwards Syndrome

Questão 11

Questão
Which of the following would result in a phenotypically normal individual?
Responda
  • Robertsonian translocation
  • Deletion
  • Duplication
  • Isochromosome

Questão 12

Questão
Which of the following would describe a male with a balanced reciprocal translocation involving 3q and 17p?
Responda
  • 44 Structurally normal chromosomes
  • An abnormal phenotype
  • No increased risk of miscarriage
  • 1 structurally abnormal chromosome

Questão 13

Questão
A 4 month old female infant is not obtaining normal developmental milestones and has failure to thrive. Chromosome analysis reveals an abnormality; one copy of chromosome 21 has extra genetic material attached to the long arm. The origin of the extra material is not obvious. All other chromosomes appear normal. How would you interpret this finding?
Responda
  • She has down syndrome
  • She has a partial trisomy 21
  • This was inherited from one of her parents who has a balanced abnormal segregation.
  • The abnormality could be phenotypically mild.

Questão 14

Questão
A monosomy is worse than a trisomy.
Responda
  • True
  • False

Questão 15

Questão
A baby is born with only one chromosome 15 with the two q arms attached at one centromere. Which of the following most correctly describes the baby's condition.
Responda
  • Robertsonian translocation
  • An unbalanced structural mutation
  • Mosaicism for chromosome 15
  • Monosomy for chromosome 15

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