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Lyrx [107]
2 years ago
14

Thick mucous gland secretions, elevated sweat electrolytes, meconium ileus, and difficulty maintaining and gaining weight are as

sociated with which autosomal recessive disorder?
1. Cerebral palsy
2. Cystic fibrosis
3. Muscular dystrophy
4. Multiple sclerosis
Biology
1 answer:
Hoochie [10]2 years ago
4 0

Answer:

The correct option is the number 2. Cystic fibrosis

Explanation:

Cystic fibrosis is a hereditary disease that affects the glands that produce mucus, sweat and digestive juices, this genetic disorder makes the secretions more sticky and thick, they accumulate and produces blockage in the tubes, ducts and passages, in particular in the lungs and pancreas.

The mucus block the ducts that carry digestive enzymes from the pancreas to the small intestine. Without these digestive enzymes, the intestines are not able to completely absorb nutrients in the food. The result is often, little increase in weight and growth, intestinal obstruction, particularly in newborns (ìleo meconium), among others.

Cystic fibrosis also affects the epithelial cells of the sweat glands, children suffering from this disorder may have a kind of salt layer on the skin. They can also lose abnormally high amounts of salt when they sweat on hot days.

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sergiy2304 [10]

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The mRNA strands go to the cytoplasm to meet ribosomes so protein synthesis can start.

Explanation:

In protein synthesis, the first step is to <em>synthesize messenger RNA</em>, mRNA. The coping process of the DNA section for the desired protein is called <u><em>transcription</em></u>, and it happens in the <em>nucleus</em>. After that, it occurs <em><u>translation</u></em>, when the formed <em>mRNA moves to the </em><em>cytoplasm</em> through the nucleus membrane pores. Protein synthesis is initiated in the cytoplasm when mRNA meets a free ribosome, the primary structure for protein synthesis. Ribosomes are made of <em>protein and ribosomal RNA</em> and can be found in the r<em>ough endoplasmic reticulum</em> or floating in the <em>cytosol</em>. They read the mRNA code and add the correct amino acid using <em>transference RNA</em> to build the protein. mARN has a <em>start and end codon</em> that tells where to start and stop adding amino acids. When the ribosome reaches the end codon, it means that protein synthesis is finished. The new protein is driven to the rough endoplasmic reticulum and translocated to the lumen. Once there, the protein suffers a few modifications, one of them is <em>folding</em> to become functional. Finally, protein is transported by vesicles to the Golgi complex, and from there to its final destiny.  

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