I need to know if my diagnoses of the following symptoms are correct before I start my research:

The 5-year-old African-American male is visiting his new pediatrician for a kindergarten physical and his mom tells the nurse that she carries the ¯Sickle Cell trait and wants Marcus screened for it.
I believe due to family history the mother wants her son tested for Sickle Cell Anemia

I agree -- although this is not a diagnosis. Screening a child whose parent carries the sickle cell trait is usually done in infancy. Only that screening and a medical doctor can actually diagnose this disorder.

You are correct a screening for the sickle cell tract for Marcus.

All of my questions are only hypothetical scenarios for my class assignment and will not be used to provide a diagnoses.

Ms. Sue, yes I agree this assignment is over simplified and I am just trying my best to complete it based on the assignment instructions.

Thank you!

You are correct in assuming that the mother wants her son, Marcus, to be tested for sickle cell anemia. Sickle cell disease is a genetic disorder that primarily affects individuals of African, Mediterranean, Middle Eastern, and Indian descent. It is characterized by the presence of abnormal hemoglobin in red blood cells, which can cause them to take on a sickle shape.

To confirm your diagnosis and further research, I would recommend the following steps:

1. Consult a healthcare professional: It's important to consult Marcus's new pediatrician, as mentioned in the context. They will have the necessary expertise and knowledge to evaluate Marcus's family history and conduct the appropriate diagnostic tests.

2. Family history assessment: Sickle cell anemia is an inherited disorder, so understanding the family history is crucial. The mother's disclosure about carrying the sickle cell trait is an important indicator that Marcus could potentially have sickle cell disease.

3. Genetic testing: Genetic testing is the most accurate way to diagnose sickle cell disease. This typically involves analyzing a blood sample to determine if the hemoglobin gene mutations associated with sickle cell disease are present.

It is important to remember that only a healthcare professional can accurately diagnose sickle cell anemia. They will consider Marcus's family history, conduct the necessary tests, and provide the appropriate guidance and support based on the results.