Thalassemia minor - Study guides, Class notes & Summaries
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NP AANP Adult Gero Boards Questions and Answers Fully solved 2023
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NP AANP Adult Gero Boards Questions and Answers Fully solved 2023 
What are the conditions needed for RBC Formation? - ANS ️️ -Functional 
Erythropoietin mechanism (90% from kidney, 10% hepatic production) 
----Erythropoietin supply is diminished in advancing renal failure, usually 
beginning with GFR< 
-Uncompromised DNA Synthesis 
---- Chronic inflammation, from autoimmune disorders (systemic lupus 
erythematous, rheumatoid arthritis and chronic infection) 
-Hemoglobin synthesis unimpai...
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MLT License Exam Questions And Answers, Latest Updated 2024/2025 )100% Correct Answers)
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MLT License Exam Questions And Answers, Latest Updated 2024/2025 )100% Correct Answers) The name of the rapid test seen in the image, often used to differentiate S. pneumoniae 
from viridans streptococci, in which a drop of 10% deoxycholate was placed on an area of 
growth, is: 
A) Bile solubility test 
B) Bile esculin hydrolysis 
C) Optochin susceptibility test 
D) Bacitracin susceptibility test - ANSWER A) Bile solubility test 
Which of the following describes the Westgard multi-rule R4S? 
A) ...
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FAMILY NURSE PRACTITIONER LABS ANCC EXAM PREPARATION QUESTIONS AND ANSWERS
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FAMILY NURSE PRACTITIONER LABS ANCC EXAM PREPARATION QUESTIONS AND ANSWERS 
 
Hgb male - ANS 13.5 to 17.5 g/dL 
 
Hgb female - ANS 12.0 to 15.5 g/dl 
 
female 
male - ANS 36% to 46 % 
41% to 53% 
 
MCV (size of RBC) - ANS 80 to100 fL >100 fl (macrocytic anemia) such as B12 deficiency (due to pernicious anemia) or folate 
 
deficiency <80 (microcytic anemia) such as iron deficiency or thalassemia trait 
 
Platelet count 
 
 . - ANS 140 − 415 × 103/mL 
 Thrombocytopenia i...
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Hematology MLS Exam Questions & Answers Graded A 2023
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The following are compounds formed in heme synthesis: 
coproporphyrinogen, porphobilinogen, uroporphyrinogen, protoporphyrinogen. 
What are the correct order in which they are formed? - porpho, uroporphy, copro, 
proto 
Which of the following is true about megakaryocytes in a bone marrow? 
a. an average of 2-10 should be found in LPF. 
b. the majority of forms are MK1 stage. 
c. morphology must be determined from Bx section. 
d. Quant. estimation done using 100x oil immersion. - a. 2-10 found in...
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FAMILY NURSE PRACTITIONER LABS ANCC EXAM PREPARATION 100% VERIFIED SOLUTIONS 2023//2024
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FAMILY NURSE 
PRACTITIONER 
LABS ANCC EXAM 
PREPARATION 100% 
VERIFIED SOLUTIONS 
2023//2024 
Hgb male - ANSWER 13.5 to 17.5 g/dL 
Hgb female - ANSWER 12.0 to 15.5 g/dl 
female 
male - ANSWER 36% to 46 % 
41% to 53% 
MCV (size of RBC) - ANSWER 80 to100 fL >100 fl (macrocytic anemia) such as B12 
deficiency (due to pernicious anemia) or folate 
deficiency <80 (microcytic anemia) such as iron deficiency or thalassemia trait 
Platelet count 
. - ANSWER 140 − 415 × 103/mL 
Thrombocytop...
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MLT ASCP Practice Questions 3.7.16 Correct Questions & Answers
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If the dilution is 1:100, and the average platelet count from both sides of the hemacytometer counting chamber in 2 mm2 is 68, what is the calculated platelet count? 
 
A. 680,000/mm3 
B. 6,800/mm3 
C. 68,000/mm3 
D. 680/mm3 
E. 34,000/mm3 - ANSWER C; 
A simple way to calculate platelet counts on the hemacytometer is to multiply the average platelet count between the two sides of the chamber by 1,000. In this case 68 x 1,000 = 68,000 platelets. The longer derivation is as follows: 
The standard ...
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USMLE step 1 – heme-onc Exam Questions with Latest Update
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measure of extrinsic clotting pathway - Answer-PT 
 
measure of intrinsic clotting pathway - Answer-PTT 
 
elevated PT and PTT - Answer-vitamin K deficiency 
DIC 
 
Glu-->Val point mutation - Answer-sickle cell disease 
 
elevated γ hemoglobin - Answer-HbF: beta thalassemia major, sickle cell disease 
bart's Hb: hydrops fetalis alpha thalassemia 
 
elevated δ hemoglobin - Answer-HbA2: beta thalassemia major and minor 
 
β4 hemoglobin - Answer-HbH: alpha thalassemia (--/-a) 
 
γ4 hemoglob...
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Fitzgerald Leik FNP Hematology exam questions and answers
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Chronic Low Volume Blood Loss: Mechanism 
-Erosive Gastritis, menorrhagia, GI malignancym & others, resulting in iron deficiency anemia 
-Iron from RBCs wasted via blood loss cannot be recycled. Clinically significant blood loss can be as little as a few mL/day 
 
 
Reduced RBC Production: Mechanism 
-Nutritional deficit (Vitamin B12, folic acid, iron deficiency), anemia of chronic disease, bone marrow suppression, reduced erythropoietin production (chronic renal failure) 
-Also associated with ...
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Thalassemia (EXAM #2) Questions And Answers 100% Verified Review A+ 2024-2025
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Thalassemia (EXAM #2) Questions And Answers 100% Verified Review A+ 
 - Synthesis of globin chains is affected - Mutations lead to decreases or absences of synthesis of the chain excesses of unaffected chains - ANS 
thalassemia 
Mutations affect alpha chains - ANS-alpha thalassemia 
Mutation affects beta chain - ANS-beta thalassemia - RBC count: normal --> increased - MCV, MCH, MCHC: decreased - Anisocytosis & poikilocytosis (target cells, basophilic stippling, may see nRBCs) - Increased ...
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AAB Hematology Board review questions and answrs(latest upate)
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Hemoglobin that has 200 times greater binding capacity for the hemoglobin molecules than oxygen? 
Carboxyhemoglobin 
 
 
 
Hemoglobin derivative that cause irreversible changes in the RBC cells 
Sulfehemoglobin 
 
 
 
Molecular structure of Hemoglobin S 
Lysine replaces glutamic acid in the 6th position of the beta chain 
 
 
 
Lab test to confirm the specific diagnosis of sickle cell anemia? 
Hemoglobin electrophoresis 
 
 
 
In Hemoglobin C what replaces glutamic acid? 
Lysine 
 
 
 
Which hem...
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