Alpha thalassemia - Study guides, Class notes & Summaries

Autosomal Dominant Correct Answer 1 parent has, 50% change of child having Autosomal Recessive Correct Answer Both parents are carriers, 25% change of child having, 50% chance child is a carrier. Cystic Fibrosis Correct Answer affects pancreas causing secretions in lungs 21st Trisomy Correct Answer Down Syndrome Klinefelter Syndrome (XXY) Correct Answer male has extra X, female like qualities Turner Syndrome Correct Answer Missing X in females Alpha Thalassemia Correct Answer i...

Family Medicine EOR: Hematology (Smarty PANCE) Exam Questions and Answers 100% Correct | Latest Version Normal or ↓ MCV, ↓ TIBC, ↑ Ferritin (high iron stores) ↓ serum erythropoietin Anemia of chronic disease The only anemia where all three cell lines are decreased (pancytopenia) ↓ WBC, ↓ RBC, ↓ Platelets - will have normal MCV and ↓ Retic Aplastic anemia ↓ Folate, ↑ MCV (macrocytic anemia) looks like B12 but no neurologic symptoms. Common in alcoholics Folate defici...

Autosomal Dominant (Ans- 1 parent has, 50% change of child having Autosomal Recessive (Ans- Both parents are carriers, 25% change of child having, 50% chance child is a carrier. Cystic Fibrosis (Ans- affects pancreas causing secretions in lungs 21st Trisomy (Ans- Down Syndrome Klinefelter Syndrome (XXY) (Ans- male has extra X, female like qualities Turner Syndrome (Ans- Missing X in females Alpha Thalassemia (Ans- inherited blood disorder; mild to severe anemia ...

Decreased TIBC, Increased Ferritin, normocytic CORRECT ANSWER Anemia of chronic dz Increased TIBC and decreased Ferritin, MCV less than 80 CORRECT ANSWER IDA Hypersegmented neutrophils CORRECT ANSWER Megaloblastic anemia (B12, folate deficiency) Increased MMA, increased homocysteine, MCV over 115, neuro symptoms CORRECT ANSWER B12 defiency PPIs, metformin, vegan, pernicious anemia are causes of CORRECT ANSWER B12 defiency Pregnancy, B12, folate, hypothyroidism, alcoholism all caus...

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) ...

MMSC433 Exam 2 Questions & Answers Already Passed Patients who are heterozygous for Hb Lepore have a clinical course: a. similar to that of alpha thalassemia minor b. similar to that of beta thalassemia minor c. similar to that of beta thalassemia major d. that is completely benign - ️️ similar to that of beta thalassemia minor What of the following is a false statement regarding the alpha thalassemias? a. beta chains are in excess in utero b. Hgb Barts can form c. gamma chains are ...

Autosomal Dominant 1 parent has, 50% change of child having Autosomal Recessive Both parents are carriers, 25% change of child having, 50% chance child is a carrier. Cystic Fibrosis affects pancreas causing secretions in lungs 21st Trisomy Down Syndrome Klinefelter Syndrome (XXY) male has extra X, female like qualities Turner Syndrome Master01 | October, 2024/2025 | Latest update 1 | P a g e | © copyright 2024/2025 | Grade A+ Missing X in females Alpha Thalassemia inheri...

Hematology Exam 2 Module MLT-MLS UAMS | Latest Update | 2024/2025 | Already Passed A Sickle Cell has: Abnormal globin chain synthesis Acanthocytes image spur cells Adult Hemoglobin Beta chain production rises gradually prenatally and reaches adult percentages between 3 - 6 months postnatally All normal adult hemoglobins are formed as tetramers consisting of 2 alpha chains 2 non-alpha chains - beta, delta, or gamma Hydrogen bonds and salt bridges an Ovalocyte has: an altered ...

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...

Family Medicine EOR: Hematology (Smarty PANCE) Exam Questions and Answers 100% Correct | Latest Version Normal or ↓ MCV, ↓ TIBC, ↑ Ferritin (high iron stores) ↓ serum erythropoietin Anemia of chronic disease The only anemia where all three cell lines are decreased (pancytopenia) ↓ WBC, ↓ RBC, ↓ Platelets - will have normal MCV and ↓ Retic Aplastic anemia ↓ Folate, ↑ MCV (macrocytic anemia) looks like B12 but no neurologic symptoms. Common in alcoholics Folate defici...