Presentation On gaucher’s disease

Slides:



Advertisements
Similar presentations
Gaucher Disease By: Melissa Sanders.
Advertisements

SICKLE CELL DISEASE Sickle cell anemia.
BLOOD DISORDERS. ANEMIA Iron-Deficiency Anemia (most common) Aplastic Anemia – bone marrow does not produce enough RBC Hemorrhagic anemia – due to extreme.
BLOOD DISORDERS. Carbon Monoxide Poisoning CO binds to your hemoglobin, prevents oxygen from binding. Can be fatal. It is a "silent killer" as people.
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: Alejandra Arellano
Sickle Cell Anemia Columbia County Medical Assistant Association.
Blood Cell Production Bone Marrow Soft, fatty, vascular tissue that fills most bone cavities It is the place where new blood cells are produced. There.
A Proteopathy Disease: Gaucher’s Disease
 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.
MUTATIONS AND GENETIC DISEASES PART 4. V. GENETIC CONDITIONS 1.Genetic Abnormality – rare condition with little or no ill effects - Ex. Six fingers, albino,
Gaucher Awareness My story By: Emma Goldstein. About Me I leave early every other Tuesday to get infusions I have a rare disease called Gaucher I get.
Dan Lauser Period 1.  Leukemia is cancer of the blood cells. It causes many problems and is very dangerous. This disease causes the bone marrow(the part.
What Really is Tay-Sachs Disease? By Aaron Husband.
Genetic Disorders and Birth Defects. Cleft lip/pallet Affects: anyone, more common in asians and native americans When appears: birth Method of inheritance:
LO: Be able to describe what gene therapy is and how it could be used.
Wellness and Illness. Cell Pathology Cell Pathology –understanding dysfunction of the body’s heirarchy dysfunction –studied at the microscope level 1)
Chronic Non-Infectious: Cancer
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.
Wilson’s Disease Yurani Farfan Mr. Trefz Genetics.
Color Blindness (#2). . Sickle Cell Anemia Affects the B-chain of Hemoglobin. It is a genetically inherited disease, and is seen commonly in Africa. Sickle.
What is sickle cell disease? Sickle cell disease is a disorder that affects.
BLOOD DISORDERS.
By: Glenna, Savannah, and Chris
Liver disease Meghan Ooten.
Basic Patterns of Human Inheritance Section 11.1 Page 296.
Is Cancer Really that Dangerous? Cause of Death Lifetime odds of dying Car Crash1 in 242 Drowning1 in 1,028 Plane Crash1 in 4,608 Lightning1 in 71,501.
Thalassemia Thalassemia is among the most common inherited disorders.
A blood disorder Ray Rega, Ryan Molter, Ryan Kosciolek.
By: Juan Carlos Bujanda. Symptoms A lot of life-threatening infections that are not easily treated and do not respond to medications, including the following:
Leukemia.
LYSOSOMES By: Carmelitta Oakley.
Cancer – A general term for more than 250 diseases characterized by abnormal and uncontrolled growth of cells.
Leukemia By: Gabie Gomez. What is Leukemia? Blood consists of plasma and three types of cells, each type has a special function. RBC, WBC and Platelets.
What is... Gene Therapy?. Genes Specific sequence of bases that encode instructions on how to make genes. Genes are passed on from parent to child. When.
G AUCHER D ISEASE Mary Jauch Persson. D IFFERENT TYPES OF THE DIEASE Type 1-childhood (most common) Enlarge liver Low blood cell level Anaemia Tiredness.
Wilson’s Disease Yurani Farfan Mr. Trefz Genetics.
Thalassemia Ms. Hoge Jane Doe. What is Thalassemia Blood disorder that is inherited, in which the body makes an abnormal form of hemoglobin. - hemoglobin.
MLAB 1315-Hematology Keri Brophy-Martinez Unit 26: Lipid Storage Diseases.
Where did Tay-Sachs come from && What is it? The disease Tay-Sachs was named after Warren Tay [ ] and Bernard Sachs[ ]. Tay-Sachs is.
Blood Disorders and Diseases -Diagnosed by a Blood Count Test - Caused by inheritance, environmental factors, poor diet, old age.
By: Ashlynn Hill. Patrice Thompson  3 year who is battling leukemia.  The doctors suggest a bone marrow transplants for a long term survival.  Neither.
By Sarah Moudy Also known as Glucocerebrosidase deficiency.
Tay-Sachs Drew Sivertsen. History Tay-Sachs is named after two physicians Warren Tay – was an ophthalmologist who was the first to discover a red dot.
Digestive System Disorders By Adrienne, Lacey, and Lindsey.
Sickle-Cell Anemia Katie Baska. What is Sickle-cell Anemia? An inherited disease that results in the production of abnormal hemoglobin in red blood cells.
1.Is NS-NPD caused by defect in a single gene or is more than one gene involved? Mutations in the NPC1, NPC2, and SMPD1 genes cause Niemann-Pick disease.
Tay-Sachs disease By Marco Rabello July/2005 NS 215 Dr.Williams.
BLOOD DISORDERS. 1. Carbon Monoxide Poisoning CO binds to your hemoglobin, prevents oxygen from binding. Can be fatal. It is a "silent killer" as people.
Cystic Fibrosis By:YaYPhineas(Edward). What is Cystic Fibrosis? A genetic disorder that affects your digestive and respiratory system You inherit a defective.
Some Genetic Disorders
3.1 Review PBS.
Blood Disorders.
Human Genetic Diseases
Review - Anemias/WBCs.
Sickle Cell anemia  .
Cancer Cancer – A general term for more than 250 diseases characterized by abnormal and uncontrolled growth of cells.
What is ... Gene Therapy?.
Tracking Genetic Traits: How it’s done!
3.1 Review PBS.
The Human Genome Chapter 14.
BLOOD DISORDERS.
BLOOD DISORDERS.
Genetics of Parenthood Quiz
Human Genetic Diseases
Gaucher Disease (this is a hereditary disease)
Single gene disorders Autosomal disorders.
Mutations.
PHENYLKETONURIA (PKU) BY: BORA LUCAJ.
Presentation transcript:

Presentation On gaucher’s disease www.AssignmentPoint.com

Gaucher's disease : Gaucher's disease is a rare genetic diseases involving a deficiency of an enzyme glucocerebrosidase which normally break down certain body glycolipids. www.AssignmentPoint.com

Types : There are 3 types of gaucher’s diseases. Type 1. Type 2. www.AssignmentPoint.com

Genetic causes : Mutation of the GBA gene leads to deficiency of an enzyme, glucocerebrosidase,which is needed to break down a lipid called glucocerebroside. This fatty substance then accumulates in "Gaucher cells" which are found particularly in the liver, spleen, and bone marrow. Damage in these organs that cause disease. Both parents must be carriers in order for a child to be affected. If both parents are carriers, 25%, chance with each pregnancy for an affected child. www.AssignmentPoint.com

symptoms of Gaucher’s diseases : Acute bone infarctions & Bone pain. Anemia &Low blood platelets. Loss of appetite. Fatigue Yellow fatty deposits on the white of the eye. Enlarged spleen and liver. Liver malfunction. Skeletal disorders. Swelling of adjacent joints. Distended abdomen. Growth retardation in children. www.AssignmentPoint.com

diagnoses : Enzyme testing DNA testing www.AssignmentPoint.com

Type 1 Gaucher’s disease : Type I the most common, also called the "non-neuropathic .It does not affect the nervous system.It affects the spleen, liver, and bone marrow .The symptoms enlargement of the spleen (the first sign),increased skin pigmentation. www.AssignmentPoint.com

Type 2 Gaucher’s disease : Type 2 Gaucher’s disease is a very rare, progessive form of Gaucher’s disease which affects the brain (central nervous system) as well as the spleen, liver, lungs and bones. Type II is characterized by neurological problems in small children. www.AssignmentPoint.com

Type-3 Gaucher’s disease : In type 3 Gaucher’s disease there neurological involvement but it is not as severe as that seen in type 2. www.AssignmentPoint.com

Treatment : Enzyme replacement treatment decrease liver and spleen size, reduce skeletal abnormalities & reverse other. Successful bone marrow transplantation. Surgery to remove the spleen. Joint replacement surgery to improve mobility & quality of life. Other treatment options include antibiotics for infections. There is currently no effective treatment for the severe brain damage that may occur in types 2 Gaucher’s disease. Gene therapy may be a future step. www.AssignmentPoint.com

…..Thank you all….. www.AssignmentPoint.com