'Fetal hemoglobin' presentation slideshows

Normal pregnancy and birth defects

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Blood (chapter 15 of your textbook)

Blood (chapter 15 of your textbook). Topics. What is blood for? How much blood? Hematocrit and anemia The constituents of plasma Red Blood Cells White Blood cells and the defensive role of blood (optional) Clotting cascades.

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Diseases of the blood

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Lateral Plate Mesoderm and Endoderm

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Globins

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Respiratory System and Gas Exchange

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Hydroxyurea

Hydroxyurea. Sahar Habibollah 18/09/08. Contents . Chemical formula Mechanism of Action Pharmacokinetics Indications Contraindications Side effects Therapeutic considerations. Hydroxyurea. Cytotoxic drug- Antimetabollite. Hydroxycarbamide . White crystalline powder Chemical formula.

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Hemo Part 2: You drive!

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Sickle Cell Disease

Sickle Cell Disease. Paolo Aquino, M.D., M.P.H., PGY I Combined Internal Medicine/Pediatrics. Outline. What is sickle cell disease? Epidemiology Manifestations Approach Treatment. What is it?.

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Isaiah 40:4, 5

Isaiah 40:4, 5 4 Every valley shall be exalted, and every mountain and hill shall be made low: and the crooked shall be made straight, and the rough places plain: 5 And the glory of the LORD shall be revealed, and all flesh shall see it together: for the mouth of the LORD hath spoken it.

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H6 Gas exchange

H6 Gas exchange. Assessment Statements. H.6.1 Define partial pressure . H.6.2 Explain the oxygen dissociation curves of adult hemoglobin , fetal hemoglobin and myoglobin.

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Chapter 7 Hemoglobin: Portrait of a Protein in Action

Chapter 7 Hemoglobin: Portrait of a Protein in Action. Heme = Fe 2+ (ferrous) + Protoporphyrin Protoporphyrin = 4 pyrrole rings + 4 methine bridges + 4 methyl groups + 2 vinyl groups + 2 propionate side chains

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THALASSEMIA

THALASSEMIA. FATIMA DARAKHSHAN (2K10-BS-V&I-35). INTRODUCTION. Inherited blood disorder an abnormal form of hemoglobin due to a defect through a genetic mutation or deletion . Results in excessive destruction of red blood cells, which leads to anemia. Types Of Thalassemia. Two types :

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Correcting Sickle-Cell Anemia

Correcting Sickle-Cell Anemia . Group B4 Jessica Hambrick Yichen Wang Tyler Fernandez Shawn Haley. Introduction. Hemoglobin : Oxygen-carrying protein Makes up Mammalian red blood cells Tetramer: contains 4 polypeptides (Freeman 2011). http://www.wikipedia.org/. (Freeman 2011).

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Sickle Cell Anemia

Sickle Cell Anemia. BY: SARA ELGHARABLI. What is Sickle Cell Anemia?. a non-contagious, hereditary disorder affecting the hemoglobin a blood disorder inherited as an autosomal recessive trait Hemoglobin is the oxygen-carrying substance in red blood cells

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Structure-Function relationship

Structure-Function relationship. Nafith Abu Tarboush DDS, MSc, PhD natarboush@ju.edu.jo www.facebook.com/natarboush. The heme. Myoglobin. The first to be determined structurally A single polypeptide chain (153 a.a ) A single heme in a hydrophobic pocket 8 ? -helices; no ? -sheets

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Hemoglobin F Quantitation Fetal Hemoglobin

Practical Hematology Lab. - LAB 8 -. Hemoglobin F Quantitation Fetal Hemoglobin. Definition :. Is the main oxygen transport protein in the fetus during the last seven months of development in the uterus and in the newborn until roughly 6 months old.

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Sickle Cell Anemia

Sickle Cell Anemia. Kristi Maulding & Matt Isenburg. Definitions . An abnormality on the structure of hemoglobin that causes red blood cells to elongate and become sickle shaped instead of being round and smooth. Symptoms .

1.28k views • 7 slides