Hemoglobinopathie Samenvattingen, Aantekeningen en Examens

Hemoglobinopathies Exam Questions And Answers 1 / 23 Hemochromatosis which gene mutation causes hemochromatosis homozygous or heterozygous are affected hemosiderin what are the main organs mostly affected by hemochomatosis genetic inheritied condition of excessive iron accumulation resulting in tissue damage HFE gene homozygous (rare) an iron-storage protein primarily made in times of iron overload liver and pancrease are main others are: heart, adrenals, testes, pi...

Hemoglobinopathies Exam Questions And Answers 1 / 23 Hemochromatosis which gene mutation causes hemochromatosis homozygous or heterozygous are affected hemosiderin what are the main organs mostly affected by hemochomatosis genetic inheritied condition of excessive iron accumulation resulting in tissue damage HFE gene homozygous (rare) an iron-storage protein primarily made in times of iron overload liver and pancrease are main others are: heart, adrenals, testes, pi...

hemoglobinopathy correct answers A genetic point mutation resulting in one nucleotide and a single amino acid substitution, addition or deletion in the globin chain that functionally changes the Hb molecule. Hb S Hb C Hb E correct answers What are the three more common hemoglobinopathies? Hb D Hb M Hb SC Hb SD correct answers What are the less common hemoglobinopathies? hemoglobin S correct answers A genetic mutation that results in an amino acid substitution yielding a hemoglobin ...

Abnormalities in structure or synthesis of hgb molecule - ANSWER-What is the cause of hemoglobinopathies? Deletions or substitutions in globin chains - ANSWER-Qualitative defects result in what? Sickle cell anemia - ANSWER-What is the most common hemoglobinopathy? 1. Class of globin chain involved 2. Severity of hemolysis 3. Compensatory globin chains - ANSWER-Hemoglobinopathy presentation depends on: beta - ANSWER-Most hgb variants are seen on which globin chain? Hgb electrophoresis - ...

SBB Hemoglobin and Hemoglobinopathies Hemoglobin tetramer - correct answer 2 alpha like chains 2 beta like chains 4 heme rings with Fe Embryonic hemoglobins - correct answer Hb Gower 1 Hb Gower 2 Hb Portland Fetal Hemoglobin - correct answer Hb F (alpha2, gamma2) Adult hemoglobin - correct answer Hb A (alpha2beta2) Hb A2 (alpha2delta2) Hemoglobin A structure - correct answer -2 alpha and 2 beta globin chains, each with a attached heme ring (Fe in center) Main function of Hb ...

puntsgewijze samenvatting

Deze samenvatting vat boek 1 en 2 van Heron - Klinische chemie en hematologie voor analisten, samen.

Uitgewerkte OWG over de fysiologie en pathologie van het hemoglobine, hemoglobinopathiën en anemie Inclusief probleemstelling en leerdoelen.

Samenvatting voor verloskunde studenten: hemoglobinopathieën en irregulaire antistoffen tijdens de zwangerschap. Onderwerpen: - Thalassemie (alfa en bèta) - Sikkelcelziekte - FMT - ADCC test - AB0-antagonisme - Resusantagonisme - Kell en duffy antagonisme

SBB Hemoglobin and Hemoglobinopathies Q&A