ASSIGNMENT HELP | In this assignment, you will research a genetic disorder, its inheritance, symptoms, diagnosis, and treatment.

This is the Critical Assignment for Bio143L.

In this assignment, you will research a genetic disorder, its inheritance, symptoms, diagnosis, and treatment. Student will write a 3-5 research paper in MLA format, while including all dimensions of the critical assignment “Rubric”, a title page, and a reference page. This is the Critical Assignment for this course and must be passed at an acceptable rate in order to pass the course. | PLACE YOUR ORDER NOW AT writtask.com |

MODEL ANSWER

Genetic Disorder: Sickle Cell Anaemia

A genetic disorder refers to a health condition resulting from abnormalities such as mutations and other changes in an individual’s | PLACE YOUR ORDER NOW AT writtask.com | common genetic disorders is sickle cell anaemia, which affects 1 in every 625 | PLACE YOUR ORDER NOW AT writtask.com | is a blood disorder created by abnormal haemoglobin, present in a person’s DNA. This disease gets its name from the shape of the red blood cells, which look like a c-shaped farm tool | PLACE YOUR ORDER NOW AT writtask.com | is also known as HbS disease, sickling disease and Hemoglobin S disease.

Inheritance

Sickle cell anaemia is an inherited disorder, a condition resulting from lack of enough and healthy red blood cells to carry oxygen needed by the body. Besides, these rigid sticky cells constantly get stuck in the small blood vessels slowing the flow of blood and oxygen to the body. Its inheritance is by the autosomal recessive pattern, which means that two copies of the abnormal DNA have to be present for the sickle cell disease to develop in a person. This means that the disorder can be passed on by two | PLACE YOUR ORDER NOW AT writtask.com | of the carrier is hardly ever affected | PLACE YOUR ORDER NOW AT writtask.com | they have a recessive gene and a dominant | PLACE YOUR ORDER NOW AT writtask.com | of the affected individual each have a copy of the mutated gene but show no symptoms of the condition. As a result, the parents would be referred to as carriers of the sickle cell trait. If two people with the trait have a child, there is a 25% chance that the child will have sickle | PLACE YOUR ORDER NOW AT writtask.com | chance that the child will be a carrier like each of its parents and a 25% likelihood that the child will neither be a carrier nor have the condition. 

Symptoms

The signs and symptoms associated with sickle cell anaemia vary from individual to individual as well as change over time. They also tend to appear at around five months of age | PLACE YOUR ORDER NOW AT writtask.com | associated with this condition is anaemia, due to the shortage of red blood cells in the | PLACE YOUR ORDER NOW AT writtask.com | red blood cells in the body, it is | PLACE YOUR ORDER NOW AT writtask.com | possible to get enough oxygen flowing throughout the body hence causing fatigue. Secondly, an individual is prone to swelling of the hands and feet, due to the blockage caused by the rigid cells in the blood vessels. An individual may also experience delayed puberty | PLACE YOUR ORDER NOW AT writtask.com | the body is not able to receive the needed oxygen and nutrients required, due to the shortage of healthy red blood cells. Vision problems are also…