Search Header Logo

Sickle Cell Symptoms/Complications/Types

Authored by Ian sharp

Biology

9th - 12th Grade

Used 10+ times

Sickle Cell Symptoms/Complications/Types
AI

AI Actions

Add similar questions

Adjust reading levels

Convert to real-world scenario

Translate activity

More...

    Content View

    Student View

6 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

1 min • 1 pt

Symptoms of sickle cell anemia usually show up at a young age. They may appear in babies as early as 4 months old, but generally occur around the 6-month mark.

While there are multiple types of SCD, they all have similar symptoms, which vary in severity. These include:

Sleep walking and active movement during sleep

swelling and pain in hands and feet, frequent infections, jaundice, which is yellowing of the eyes and skin

Rashes and are frequent and severely painful

2.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

This type if Sickle Cell Disease involves the beta globin gene. It has similar symptoms to Hb SS anemia. However, sometimes the symptoms of beta zero thalassemia are more severe. It is associated with a poorer prognosis.

Hemoglobin SB+ (beta) thalassemia

Hemoglobin SD, hemoglobin SE, and hemoglobin SO

Hemoglobin SB 0 (Beta-zero) thalassemia

Hemoglobin SC disease

Hemoglobin SS disease

3.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

This type if Sickle Cell Disease is the most common type of sickle cell disease. It occurs when you inherit copies of the hemoglobin S gene from both parents. This forms hemoglobin known as Hb SS. As the most severe form of SCD, individuals with this form also experience the worst symptoms at a higher rate.

Hemoglobin SB+ (beta) thalassemia

Hemoglobin SD, hemoglobin SE, and hemoglobin SO

Hemoglobin SB 0 (Beta-zero) thalassemia

Hemoglobin SC disease

Hemoglobin SS disease

4.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

This type if Sickle Cell Disease is the second most common type of sickle cell disease. It occurs when you inherit the Hb C gene from one parent and the Hb S gene from the other. Individuals with Hb SC have similar symptoms to individuals with Hb SS. However, the anemia is less severe.

Hemoglobin SB+ (beta) thalassemia

Hemoglobin SD, hemoglobin SE, and hemoglobin SO

Hemoglobin SB 0 (Beta-zero) thalassemia

Hemoglobin SC disease

Hemoglobin SS disease

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Children are only at risk for sickle cell disease if both parents carry sickle cell trait. A blood test called a hemoglobin electrophoresis can also determine which type you might carry.

People from the following regions have endemic malaria are more likely to be carriers. This includes people from:

Africa, India, Unites States, Canada

Africa, India, Canada, South America

the Mediterranean, Northern Ireland, Germany

Saudi Arabia, Africa, India, The Mediterranean

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

SCD can cause severe complications, which appear when the sickle cells block vessels in different areas of the body. Painful or damaging blockages are called sickle cell crises. They can be caused by a variety of circumstances, including:

illness, changes in temperature, stress, poor hydration, altitude

sugary food, too much sleep, mood swings

alcohol consumption, ringing in the ears (tinnitus)

Access all questions and much more by creating a free account

Create resources

Host any resource

Get auto-graded reports

Google

Continue with Google

Email

Continue with Email

Classlink

Continue with Classlink

Clever

Continue with Clever

or continue with

Microsoft

Microsoft

Apple

Apple

Others

Others

Already have an account?