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Romashka [77]
3 years ago
14

What is. . .

Biology
1 answer:
Airida [17]3 years ago
7 0

the answer is chemical reaction

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Lesch-Nyhan syndrome is an X-linked, recessive condition caused by mutation of the HPRT1 gene responsible for purine metabolism.
Elanso [62]

Answer:

B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.

A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.

Explanation:

As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.

The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.

As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.

3 0
3 years ago
This type of agent kills bacteria, fungi, and viruses—even normal cells or abnormal cancer cells.
melomori [17]
It is the destructive agent 
4 0
3 years ago
Digeorge syndrome is characterized by a cleft palate, immune deficiency, and developmental issues. which chromosomal change caus
Temka [501]

The correct answer is Deletion.

DiGeorge syndrome, more commonly considered as 22q11.2 deletion syndrome. It refers to an ailment resulting when a small segment of chromosome 22 is missing. This deletion leads to poor development of many systems of the body.

The medical issues generally associated with 22q11.2 deletion syndrome involve poor immune system function, heart defects, a cleft palate, delayed development with emotional and behavioral issues, and issues associated with diminished levels of calcium in the blood.


7 0
3 years ago
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What type of bonds within the tertiary structure of an enzyme will break at high temperatures? Which bonds will not break?
Korolek [52]

Answer:

The bonds that will break at high temperature are hydrogen, ionic and Van der Waal's interactions. Covalent bonds will not break.

Explanation:

6 0
3 years ago
An image formed by a mirror with a flat surface is called a(n) ________ image
Inessa05 [86]
It Is called, a mirror image or reflection.
5 0
3 years ago
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