Sickle ce - Study guides, Class notes & Summaries
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Sickle Cell Anemia questions with correct answers
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What is sickle cell anemia? - Answer An autosomal recessive disorder resulting in a mutated form of hemoglobin (HbS) 
 
What causes sickle cell TRAIT? - Answer ONE allele on the beta globin gene carries the sickle mutation, one normal allele for HbA (heterozygous) 
 
What causes sickle cell DISEASE? - Answer TWO alleles on the beta globin gene carries mutation for sickle mutation (homozygous) 
 
What does the sickle cell mutation cause resistance to? - Answer Plasmodium falciparum (malar...
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Sickle Cell Disease questions with correct answers
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Sickle Cell Disease - Answer Is a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells. 
 
Risk Factors for Sickle Cell Disease Include - Answer 1-Genetics: Having parents heterozygous for hemoglobin S 
 
2-Ethnicity: Been of African American descent 
 
Other races that can be affected are people from Mediterranean , Caribbean, Arabian, and east Indian descent. 
 
Hemoglobin S is Sensitive t...
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NURSING 5327 mod 5 case study sickle cell crisis.
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NURSING 5327 mod 5 case study sickle cell crisis.
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Sickle Cell Case Study Anthony Perkins is a 15-year-old African American
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Anthony Perkins is a 15-year-old African American male who was at a medically monitored summer camp and 
participated in several sports activities when the outside temperature was greater than 90 degrees. He began having pain in 
his knees and was evaluated by the camp nurse. After evaluation, he was transported to his primary care provider and 
evaluated. Anthony was transferred as a direct admit to the pediatric floor of the community hospital where you are the 
primary nurse responsible for h...
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Sickle Cell Anemia - ATI: Nursing Care of Children Questions & 100% Verified Answers | Latest Update | Already Graded A+
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Sickle Cell Disease ☑: a group of diseases (autosomal recessive genetic disorder) in which abnormal 
sickle hemoglobin S (HbS) replaces normal adult hemoglobin (Hgb A). 
Sickle Cell Anemia ☑: the homozygous and most common form of SCD. Increased destruction of 
RBCs occurs. 
manifestations of SCA (resultl of RBC sickling) ☑: increased blood viscosity, obstruction of blood flow, and tissue hypoxia (causes 
tissue ischemia, resulting in pain) 
when manifestations begin to appear ☑: late...
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Sickle Cell Disease questions with correct answers
- Exam (elaborations) • 10 pages • 2023
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Sickle Cell Disease - Answer Is a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells. 
 
Risk Factors for Sickle Cell Disease Include - Answer 1-Genetics: Having parents heterozygous for hemoglobin S 
 
2-Ethnicity: Been of African American descent 
 
Other races that can be affected are people from Mediterranean , Caribbean, Arabian, and east Indian descent. 
 
Hemoglobin S is Sensitive t...
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Hbss Sickle Cell Disease And Anesthesia Questions And Answers Well Elaborated Rated A+
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Hbss Sickle Cell Disease And Anesthesia Questions And Answers Well Elaborated Rated A+
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Anthony Perkins Sickle Cell Anemia Case Study-latest-2023
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Anthony Perkins Sickle Cell Anemia Case Study-latest-2023
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Sickle Cell Anemia - ATI: Nursing Care of Children Exam Questions and Answers
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Sickle Cell Anemia - ATI: Nursing Care of Children 
Exam Questions and Answers 
Sickle Cell Disease - Answer- a group of diseases (autosomal recessive genetic 
disorder) in which abnormal sickle hemoglobin S (HbS) replaces normal adult 
hemoglobin (Hgb A). 
Sickle Cell Anemia - Answer- the homozygous and most common form of SCD. 
Increased destruction of RBCs occurs. 
manifestations of SCA (resultl of RBC sickling) - Answer- increased blood viscosity, 
obstruction of blood flow, and tissue hypox...
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NUR MISC FINAL ANSWER KEY UNFOLDING Reasoning Sickle Cell Anemia Anthony Perkins, 15 years old
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NUR MISC FINAL ANSWER KEY UNFOLDING Reasoning Sickle Cell Anemia Anthony Perkins, 15 years old 
 
© 2016 Keith Rischer/www.KeithRN.com 
Sickle Cell Anemia 
Anthony Perkins, 15 years old 
Primary Concept 
Perfusion 
Interrelated Concepts (In order of emphasis) 
1. Pain 
2. Clotting 
3. Fluid and Electrolyte Balance 
4. Clinical Judgment 
5. Patient Education 
6. Communication© 2016 Keith Rischer/www.KeithRN.com 
UNFOLDING Reasoning: ANSWER KEY 
Sickle Cell Crisis 
History of Present Problem: 
A...
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