ILL MARK AS BRAINLIEST AND THANK YOU FROM THE GODS, PLEASE HELP

Introduction

Muscular dystrophy is a genetic disorder that affects a person's voluntary muscles. People with muscular dystrophy have incorrect or missing information in their genes, which prevents them from making the proteins they need for healthy muscles. Because muscular dystrophy is genetic, people are born with the problem ; it is not contagious; therefore, you can't catch it from someone else. Additionally, two people who do not have muscular dystrophy can have a child with the disorder.
Goal

To create a PowerPoint presentation for families with children recently diagnosed with muscular dystrophy.
Role

You are a family physician who was asked by a local hospital's muscular dystrophy parent support group to present to a group of parents with children recently diagnosed with muscular dystrophy.
Audience

The families with children who were recently diagnosed with muscular dystrophy.
Situation

You have been hired by the local hospital's muscular dystrophy parent support group to provide an overview of the genetic disorder including the genetic basis for the disorder, treatments, costs, and what a child can and cannot do with muscular dystrophy. You will need to reinforce the fact that muscular dystrophy is a manageable disease. A question and answer period will follow.
Performance

You need to create a PowerPoint presentation for the family about: the details/introduction of muscular dystrophy outline the genetic basis of the disorder treatment options costs impact on the child (what they can and cannot do) Graphically pleasing presentation appropriate for the target audience with text, graphics, etc . to convey your message

Respuesta :

Answer:

   Muscular dystrophy (MD) is a group of inherited diseases in which the muscles that control movement (called voluntary muscles) progressively weaken. In some forms of this disease, the heart and other organs are also affected. There are nine major forms of muscular dystrophy: Myotonic.

In most cases, muscular dystrophy (MD) runs in families. It usually develops after inheriting a faulty gene from one or both parents. MD is caused by mutations (alterations) in the genes responsible for healthy muscle structure and function.

Explanation:

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Answer:

The first historical account of muscular dystrophy appeared in 1830, when Sir Charles Bell wrote an essay about an illness that caused progressive weakness in boys. Six years later, another scientist reported on two brothers who developed generalized weakness, muscle damage, and replacement of damaged muscle tissue with fat and connective tissue. At that time the symptoms were thought to be signs of tuberculosis. In the 1850s, descriptions of boys who grew progressively weaker, lost the ability to walk, and died at an early age became more prominent in medical journals. In the following decade, French neurologist Guillaume Duchenne gave a comprehensive account of 13 boys with the most common and severe form of the disease (which now carries his name—Duchenne muscular dystrophy). It soon became evident that the disease had more than one form, and that these diseases affected people of either  and of all ages. Muscular dystrophy (MD) refers to a group of more than 30 genetic diseases that cause progressive weakness and degeneration of skeletal muscles used during voluntary movement. The word dystrophy is derived from the Greek dys, which means "difficult" or "faulty," and troph, or "nourish.

Explanation: this is one paragraph hope this helps