A structural chromosomal abnormality is described by which of the following?
Respuesta
Chromosome breakage with improper repair
Nondisjunction of chromosomes during Meiosis I
Nondisjunction of chromosomes during Meiosis II
Extra chromosomes created and added to genome
Pregunta 2
Pregunta
How many chromosomes could someone with polypoidy have?
Respuesta
69 chromosomes
47 chromosomes
45 chromosomes
Pregunta 3
Pregunta
You can survive with only one X chromosome.
Respuesta
True
False
Pregunta 4
Pregunta
Dispermy results in?
Respuesta
Triploidy
Tetraploidy
Polyploidy
Pregunta 5
Pregunta
The most common pregnancy complication is [blank_start]spontaneous abortions[blank_end].
Respuesta
spontaneous abortions
Pregunta 6
Pregunta
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?
Respuesta
Edwards Syndrome, Nondisjunction
Edwards Syndrome, Robertsonian Translocation
Patau Syndrome, Nondisjuction
Patau Syndrome, Robertsonian Translocation
Pregunta 7
Pregunta
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].
Respuesta
13
21
18
22
19
17
15
25
Pregunta 8
Pregunta
Turner Syndrome is a result of nondisjunction of maternal chromosomes.
Respuesta
True
False
Pregunta 9
Pregunta
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]
Respuesta
X
XXY
XXX
47, XYY
Pregunta 10
Pregunta
Which of the following (more than one?) could be caused by maternal nondisjuction?
Respuesta
Turner Syndrome
Triple X Syndrome
Klinefelter Syndrome
Edwards Syndrome
Pregunta 11
Pregunta
Which of the following would result in a phenotypically normal individual?
Respuesta
Robertsonian translocation
Deletion
Duplication
Isochromosome
Pregunta 12
Pregunta
Which of the following would describe a male with a balanced reciprocal translocation involving 3q and 17p?
Respuesta
44 Structurally normal chromosomes
An abnormal phenotype
No increased risk of miscarriage
1 structurally abnormal chromosome
Pregunta 13
Pregunta
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?
Respuesta
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.
Pregunta 14
Pregunta
A monosomy is worse than a trisomy.
Respuesta
True
False
Pregunta 15
Pregunta
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.