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Sagot :
Answer:
Neurofibromatosis type 1 (NF1) is a hereditary disorder caused by an alteration – called a mutation – in the NF1 gene, which is located on chromosome 17. The NF1 gene contains a code of instructions for making a protein called neurofibromin, which is produced in many cells, including nerve cells and specialized cells surrounding nerves (Schwann cells). The neurofibromin protein acts as a tumor suppressor, preventing cells from growing and dividing too rapidly. The NF1 gene mutation leads to the production of a nonfunctional or absent neurofibromin protein that is unable to regulate cell growth and division, resulting in the growth of neurofibromas (skin tumors) along nerves throughout the body.
Explanation:
As per diagnosis the kai has a disorder.
- Kai parent claims that Kai had been diagnosed with underlying cause of infections in the cells and needs to have immediate treatment
- Its a complex disorder that is created by the mutation of a gene which is responsible for the formation of the proteins. It not limited by age
- The severity of the disorder varies and there exists a 50% of chance that the parent may pass this to their offspring.
Learn more about the paragraph for Kai's parents in which you explain.
brainly.com/question/22669492.
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