Welcome to Westonci.ca, your ultimate destination for finding answers to a wide range of questions from experts. Discover a wealth of knowledge from experts across different disciplines on our comprehensive Q&A platform. Get precise and detailed answers to your questions from a knowledgeable community of experts on our Q&A platform.

20 POINTS IF WRITTEN SOON
Educate the Patient
Instructions: Write a paragraph for Kai's parents in which you explain what they need to know about Kai's diagnosis.
Include and underline or highlight each of these terms to help them understand Kai's diagnosis: NF1, inherited,
mutation, chromosome 17, gene, protein, neurofibromin, mitosis, tumors.


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.