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Aleks04 [339]
3 years ago
13

With increasing age comes a greater chance of a woman having been exposed to damaging environmental agents such as drugs, chemic

als, and radiation. These factors may act on the aging oocyte to cause which abnormality in a fetus?
Biology
2 answers:
allsm [11]3 years ago
5 0
<h2>Down Syndrome</h2>

Explanation:

Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21

  • Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
  • Down syndrome is usually caused by an error in cell division called nondisjunction which results in an embryo with three copies of chromosome 21 instead of the usual two
  • Prior to or at conception, a pair of 21st chromosomes in either the sperm or the egg fails to separates
  • With development in embryo the extra chromosome is replicated in every cell of the body;this type of Down syndrome which accounts for 95% of cases is called trisomy 21
  • Maternal age is the only factor that has been linked to an increased chance of having a baby with Down syndrome resulting from nondisjunction;here environmental agents such as drugs, chemicals, and radiation act as mutagens which induce mutation in the fetus
trasher [3.6K]3 years ago
5 0

Answer:

<h2>Down syndrome </h2>

Explanation:

Down syndrome; is a condition in which there is an extra copy of a chromosome, total chromosomes are 47 (46+1). The patient of Down syndrome contain an extra copy of 21 th chromosome. Chromosome determine how a baby's body forms during pregnancy and how the baby's body functions as it grows in the womb and after birth. Typically, a baby is born with 46 chromosomes, but in case of down syndrome, there is an extra copy of 21 number chromosome, which cause greater risk of abnormality in fetus of aging oocyte.

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Check all the functions that take place within the eukaryotic cytoplasm.
sesenic [268]

The cytoplasm is a fluid substance that fills every living cell which is enclosed by the cell membrane. This substance is mainly composed of water and proteins.

The functions that take place within the eukaryotic cytoplasm are diverse:

  • Location for most metabolic pathways. Except for the metabolic pahtways in cell nucleus and cytoplasmatic organelles, all metabolic functions (e.g., synthesis of biomolecules, growth, etc) occur in the cytoplasm.  The cytoplasm contain enzymes (i.e., proteins) to carry out different chemical reactions.

  • Location for organelles that house many of the metabolic pathways for the cell. For example, the synthesis of ATP (the energy coin of the cells) is carried out in the mitochondria, which are organelles found in the cytoplasm.

  • Location for the cytoskeleton that gives integrity to the cell. The cytoplasm contains all of the three types of filaments of the cytoskeleton (i.e., microtubules, actin filaments, and intermediate filaments) which provides structural support to the cells.

On the other hand, in plant cells, the cell wall is located outside the cell membrane.

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brainly.com/question/9492242?referrer=searchResults

7 0
2 years ago
In an experiment, a scientist studied the effect of increased levels of calcium had on a sugar levels in the blood. The scientis
ololo11 [35]

Answer:

If the calcium levels in blood increases, then there is increase in blood glucose level.

Explanation:

Calcium in blood plays a vital role of homeostasis in regards to level of secretion of insulin. If the calcium level is altered, the homeostasis mechanism is hampered. Several  researches have shown that alteration of serum calcium level affects the metabolism process of carbohydrate and makes the person vulnerable to risks of diabetes mellitus and associated complications. Hence during calcium supplementation, the person's blood glucose level must be considered.

7 0
3 years ago
Punnett Squares are used by geneticists to determine the likely genotypes of the offspring of two parents.
PilotLPTM [1.2K]
That's correct - it's a square where on one axis, the paternal allele (allele = one of the possible forms of the same gene), and on another the maternal allele is listed. Often, it's also indicated whether an allele is recessive or dominant.

Then, in the table that results, all the possible "combinations" of allele between the paternal and maternal party are created. If you count how often a certain combination appears, it indicates the likelihood of that combination.
See the picture (though it is directly from Wikipedia, please note). The likelihood of BB is 25%, of Bb is 50%, and of bb 25%.

6 0
3 years ago
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The answer we’ll be c
7 0
4 years ago
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Which of the following is an example of an X-linked recessive disorder?
yKpoI14uk [10]
An example for X-linked recessive disorder is (C). Color Blindness 
3 0
3 years ago
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