By: Juan Pablo Ordoñez, Valeria Méndez,

Slides:



Advertisements
Similar presentations
SICKLE CELL DISEASE Sickle cell anemia.
Advertisements

Iron Deficiency Anemia By: Tiffany Davis & Chanelle Washington.
WHAT IS ANEMIA? It is a condition where the red blood cells in the blood fall below normal so the body gets less oxygen resulting in weakness. We are the.
Role of iron deficiency anemia in the propagation of beta thalassemia gene Usman, M., Moinuddin, M., Ahmed, S.A. (2011) Korean J Hematol 46: Microcytic.
Sickle Cell Anemia By Alex Lange & Roy Darrah. Inheritance Pattern Parents can be carriers and show no symptoms of the disease. Sickle Cell Anemia is.
By: Breanna Parker & Jake Perkins
By: Alejandra Arellano
Sickle Cell Anemia By: Daniel Lee, Matt Milan, and Min-ki Kim.
By: Kyle Wislinsky Bryce Peterson
Mediterranean Anemia-Thalassemia
Sickle Cell Anemia. What Is It? Sickle Cell Anemia is……. A Genetic disease body produces abnormally shaped red blood cells. Red blood cells shaped like.
Beta Thalassemia by Sylvester Definition: Thalassemia is inherited disorders characterized reduced or absent amounts of hemoglobin, the oxygen-carrying.
Thalassemia & Treatment
Hemoglobin (Hb) Hb is found in RBCs its main function is to transport O2 to tissues. Structure: 2 parts : heme + globin Globin: four globin chains (2 α.
THALASSEMIA PRESENTED BY “Sir Sanjaykumar M. Vasoya” {Biotechnologist}
P. Pathophysiology Normally, the majority of adult hemoglobin (HbA) is composed of four protein chains, two α and two β globin chains arranged into.
 Your body makes three types of blood cells: red blood cells, white blood cells, and platelets (PLATE-lets). Red blood cells contain hemoglobin, an iron-rich.
Andrew Novoa and Thea De Guzman 2/1/10 Per. 3
By: Austin Schulte & Brendan Logan P. 4. Background/History  Discovered in 1910  The disease is said to have originated in Africa, but it was first.
NOTES 24 – Genetic Disorders and Hereditary Diseases
Anemia Dr Gihan Gawish.
By: Ruth Maureen Riggie
Sickle Cell Anemia Katie Coltharp and Mariela Saenz.
Blood Types.
By: Kaitlyn Fleming. What is Anemia? Anemia is a condition in which the body does not have enough healthy red blood cells. When your body does not have.
Vocabulary and Graphic Organizers
Iron Deficiency Anemia
FATIMA DARAKHSHAN (2K10-BS-V&I-35)
Anemia By: Britani Prater. What is Anemia? The red blood count is less then normal. The red blood count is different in females and males. Males
What Is Thalassemia? Thalassemia is a group of inherited disorders of hemoglobin synthesis characterized by a reduced or absent output of one or more of.
Thalassemia Jon Clapp ISAT 351 Presentation 12 April 1999.
Sickle Cell Anemia By: Virginia Myers, Emily Stein, and Caroline McGuire Mrs. Geithner-Marron Period 1 Due: Tuesday, February 8th, 2011.
Jade Rotondo March 20, 2012 Grade 7 B168.  This project is going to be about our blood that functions and transfers important things in our body. Jade.
Genetic disorders C.1.m. – Describe the mode of inheritance of commonly inherited disorders.
Sex-linked Genetic Disorders & Autosomal Disorders Packet #41 Chapter #14.
Dextrocardia By: Elizabeth Ramirez. What are genetic disorders?  Genetic disorders are problems that happen in the DNA. A part of the DNA was not reproduce.
The Medical Mystery of Sasha Fierce By: Doctors Vanessa L’Abbate, Sarah Danzinger and Lydia Torres.
Genetic Diseases L.O: To understand how some genetic diseases can be inherited Starter: list as many inherited diseases that you can think of.
Human Genetic Disorders Biology. Mutations Sometimes genes are damaged or copied incorrectly. A change in a gene is called a mutation. Mutations are a.
What is sickle cell disease? Sickle cell disease is a disorder that affects.
By: Glenna, Savannah, and Chris
Thalassemia Thalassemia is among the most common inherited disorders.
Hematological Diseases
A blood disorder Ray Rega, Ryan Molter, Ryan Kosciolek.
Thalassemia & Treatment. What is thalassemia? Genetic blood disorder resulting in a mutation or deletion of the genes that control globin production.
SICKLE CELL DISEASE (scd) By: Yousef Al Sultan Fatimah Al Khamis.
Phenylketoriuria (PKU)
SICKLE CELL ANEMIA Omar and Yassin.
 SCA  Hemoglobin  How it is acquired  Symptoms  What happens in SCA  Treatment.
+ Anaemia By Lucy Feyen. + Does Anaemia even affect many people? Yes anemia affects more than ¼ of the world, In fact in Australia, ,000.
Human Genetic Disorders
1 Sickle Cell Disease. 2 Bone marrow produces RBCs with defective hemoglobin.
What Do You Want To Know About Thalassaemia (Carrier)
Sickle Cell Disease Taeron Burrell. What Is Sickle Cell Anemia? Sickle cell Anemia is a serious disorder in which the body makes sickle shape blood cells.
Autosomal Recessive Inheritance By: Joey Cisneroz 121.
Thalassemia Ms. Hoge Jane Doe. What is Thalassemia Blood disorder that is inherited, in which the body makes an abnormal form of hemoglobin. - hemoglobin.
By: Ashlynn Hill. Patrice Thompson  3 year who is battling leukemia.  The doctors suggest a bone marrow transplants for a long term survival.  Neither.
CHISOM AMAEFUNA ADELINE LAURENTE 1/29/10 PERIOD 2 Sickle Cell Anemia.
Sickle-Cell Anemia. Symptoms Anemia: The shriveled blood cells of an individual with this disorder may break apart, causing a shortage in red blood cells,
By: Xavier Amaro, Destynee Bodrick, Armaiyah Phelps, Anayeli Ortiz SICKLE CELL DISEASE.
THALASSEMIA “SEA IN THE BLOOD” By: Marija Jukic. HIS TORY AND BACKGROUND  1925  Doctor Thomas Cooley  Genetic blood disorder  First discovered in.
PRACTICE TEACHING ON THALASSEMIA. INTRODUCTION O Inherited blood disorder O an abnormal form of hemoglobin due to a defect through a genetic mutation.
Review - Anemias/WBCs. Hemolytic Anemia Arrows indicate cells being destroyed; Acquired (thru certain chemicals) or inherited RBCs are destroyed before.
Michael Hua March 20,2012 Grade 7 B168 My project is all about blood. Blood is part of the circulatory system. Blood is important for us to live because.
GENETIC DISEASES Lecture 5
Review - Anemias/WBCs.
Methemoglobinemia Liza and Makena.
Sex-linked Genetic Disorders & Autosomal Disorders
THALASSEMIA Ahmed Salam Lectures Medical Student “TSU”
Hemolytic Anemia.
Presentation transcript:

By: Juan Pablo Ordoñez, Valeria Méndez, Thalassemia By: Juan Pablo Ordoñez, Valeria Méndez,

What is Thalassemia? Genetic disorder in which the body produces an unusual amount of hemoglobin There are several different types of thalassemia: Alpha Thalassemia Beta Thalassemia Thalassemia Intermediate Thalassemia minor

How is it inherited? The disease is inherited when both of the parents are carriers of this disorder. When only one parent has the disease the offspring develops thalassemia minor, but rarely shows symptoms.

What are the symptoms? Major Thalassemia Thalassemia Minor Anemia Usually the person will not show any physicall symptom, but they will develop smaller red blood cells. Fatigue Shortness of Breathing Yellow Skin Iron overload When the pacient is in treatment.

Treatments There is no safe cure. The most common treatment is blood transfusion, This will replace the lost red blood cells with new. It will give the patient a better quality and quantity of life. A sideffect of this treatment may be an iron overload, but it can be treated with special pills (iron chelators)

Other Facts 100,000 children are born with this defect every year (approximately) It is estimated that around 20-25 million people are carriers of this disease Europe and the Americas has a low risk 1/300 people are carriers 1/1000 are low risk And 1/30 are high risk

Bibliograohy Disease & Treatment « Thalassemia. (n.d.). Retrieved March 5, 2015, from http://www.thalassemia.ca/disease-treatment/ Holm, G. (2012, July 17). Health Line. Retrieved from http://www.healthline.com/health/thalassemia#Overview1 Plus, M. (2014, February 24). Medline Plus. Retrieved from http://www.nlm.nih.gov/medlineplus/ency/article/000587.htm