Explore the genetic and hormonal aspects of reproductive health in this quiz titled 'Block 7 Repro genetics MCQ's prt 1'. Assess your understanding of genetic mutations affecting reproductive hormones, conditions like endometriosis, and hormonal feedback mechanisms during the ovarian cycle.
Assortative mating
Allele sharing
Additive effects
Low heritability
Anticipation
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Additive effects
Shared environment
Assortative mating
Polygenic inheritance
Disruptive selection
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D
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Ischemia and necrosis of the stratum functionale is the main event.
It depends on estrogen
It starts upon arrival of ovulation
The uterine glands are highly coiled and their lumens are filled with secretions
Endocervix is sloughed off.
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The daughter of an alcoholic father
The son of an alcoholic father
The son of an alcoholic mother
The daughter of an alcoholic mother
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Over-expression of luteinizing hormone (LH) and follicle stimulating hormone (FSH).
Under-expression of gonadotropin releasing hormone (GnRH) by the paraventricular nucleus of the hypothalamus.
Over-expression of oxytocin by supraoptic neurons (SON) of the hypothalamus.
Over-expression of aromatase by granulosa cells of the ovary.
Over-expression of cholesterol side chain cleaving enzyme (also known as desmolase) by mitochondria of theca and granulosa cells of the ovary.
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B
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D
Absence of GnRH surge
Prolonged elevation of follicle stimulating hormone
Increase in plasma leptin
Absence of a surge in luteinizing hormone
Abnormally elevated plasma estradiol
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The granulosa layer of cells of a secondary follicle is highly vascularized
The theca externa produces androstenedione
The basal lamina separates the primary oocyte from the granulosa layer
The zona pellucida found in the secondary follicle is composed of GAGs and glycoproteins
The secondary follicle contains a secondary oocyte
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The recurrence risk after the birth of an affected child is close to 3%
The recurrence risk after the birth of two affected children is as high as the recurrence risk after the birth of one affected child
Concordance between identical twins is close to 100%
The recurrence risk after the birth of an affected child is not significantly increased above the population incidence
The clinical severity of the defect in an affected child is unrelated to the recurrence risk
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Measurement error
Nonadditive genes
Nonshared environment
Assortative mating
Shared environment
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Multifactorial and autosomal dominant diseases but not autosomal recessive diseases and chromosome aberrations
Autosomal recessive diseases and chromosome aberrations, but not autosomal dominant and multifactorial diseases
Autosomal dominant and autosomal recessive diseases but not multifactorial diseases and chromosome aberrations
Multifactorial and autosomal recessive diseases, but not autosomal dominant diseases and chromosome aberrations
Multifactorial diseases and chromosome aberrations but not autosomal dominant and autosomal recessive diseases
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FSH stimulates the primordial follicles to develop
LH stimulates proliferation of the granulosa layer of cells in the multilamina primary follicle
Activin stimulates proliferation of the follicular layer to form the granulosa layer in the multilaminar primary follicle
FSH inhibits the production of progesterone in the corpus luteum
LH inhibits the production of estrogen in the corpus luteum
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Nonshared environment
Assortative mating
Additive gene effects
Shared environment
Non-additive gene effects
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Complete absence of the LDL receptor
Up-regulation of the LDL receptor
Low levels of circulating plasma LDL
Low activity of HMG-CoA reductase
Excessively high plasma levels of HDL and LDL
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