Trichomoniasis is caused by a protozoan parasite that causes a mal/odorous frothy yellow to green discharge, itching (pruritus), and burning.
<h3>What is Trichomoniasis?</h3>
Trichomoniasis is a disease caused by a parasite whose symptoms are hugely variable among different persons.
Trichomoniasis is caused by the protozoan <em>Trichomonas vaginalis</em>, which infects suitable human hosts.
Trichomoniasis is a serious-mid disease and it must be treated properly in medical settings.
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The arrangement of homeotic genes along chromosomes of vertebrate and invertebrate animals corresponds to the expression pattern of the genes along the anterior-posterior axis of the developing embryo.
<h3>What are homeotic genes?</h3>
- Homeotic genes are a group of body pattern forming genes which control the development along the anterior- posterior axis of the developing embryo.
- These encode transcription factors which control and specify the genes involved in body patterning. These provide identity to the segments during embryo formation.
- Genes located in the 5’ end act on posterior side whereas the genes on 3’ end act on anterior region.
- Homeotic genes are evolutionary conserved and control body specification, patterning and differentiation.
- The loss of function of any of the gene changes the body pattern and affects the development.
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Explanation:
So when u take antibiotics you kill lots of the bacteria. however you don't kill all of them. the bacteria that is left over hasn't been killed because they are resistant to the antibiotics taken. if left these bacteria will reproduce and build and species resistant to that type of antibiotics which can be incredibly dangerous. this is why it is necessary to finish your full antibiotics course so even if u feel better just to make sure you kill all the bacteria.
The answer is (B) Edward's Syndrome, Down Syndrome, Klinefelter's Syndrome.
These syndromes are caused when there is an extra copy of chromosomes present in the cells.
In Edward's syndrome, there is an extra copy of the chromosome 18.
In Down's syndrome, there is an extra copy of chromosome 21.
In Klinefelter's syndrome, there is an extra copy of X chromosome.
