'Hemophilia' presentation slideshows

Advanced Biology

Advanced Biology. Unit 3. The Monk and his peas .

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Hemophilia

Hemophilia. Galila Zaher Consultant Hematologist MRCPath KAUH. Prevalence. World-wide occurs in all racial groups. Few decades ago, children with haemophilia had a significantly reduced life expectancy. Crippled with arthritis &joint deformity

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CAUSES OF BLEEDING

CAUSES OF BLEEDING. Defective clot formation Platelet plug Fibrin clot Excessive fibrinolysis Vascular fragility. PLATELET DEFECTS. Thrombocytopenia Increased consumption (ITP, DIC) Decreased production (marrow disease, chemo)

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19. Treatment of Genetic Diseases

19. Treatment of Genetic Diseases. Somatic Cell Gene Therapy. a). Treatment strategies i). Metabolic manipulation ii). Manipulation of the protein iii). Modification of the genome b). Strategies for gene transfer. Three categories of somatic cell gene therapy:

1.18k views • 37 slides

By Lisa Marie Meffert, Ph.D. Rice University

Pedigrees: Working Out Inheritance Patterns. By Lisa Marie Meffert, Ph.D. Rice University. Genology - Lee Family of Virginia and Maryland c1886 Apr. 26. Prints and Photographs Division, Library of Congress (LC-USZ62-90145. Factors to Consider in Pedigrees.

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The NHF-McMaster guidelines on models of care in hemophilia

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Anastasia and The Russia Revolution

Anastasia and The Russia Revolution. Ansatsia's father. Nicholas II, Last Czar of Russia. Alexis is born! Son with Hemophilia. Winter Palace. Russian Peasants. Duma.

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SEX-LINKED INHERITANCE

SEX-LINKED INHERITANCE. Objectives. Meet with Thomas Hunt Morgan Define Sex Linkage Define Sex linkage in Drasophila melaganester Describe Hemoplia , colourblidness and Muscular dystrophies. SO WHAT IS SEX LINKED INHERITANCE ??. Thomas Hunt Morgan.

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Extensions on Mendelian Genetics

Extensions on Mendelian Genetics. Genotype vs. Phenotype. Since an individual has two copies of each gene, a heterozygous individual carries the recessive gene without showing it. This is referred to as a carrier . Some human disorders are caused by recessive alleles (ex: cystic fibrosis).

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DNA and Mutations

DNA and Mutations. Mutation. Mutation - any change in the DNA. Caused by errors in DNA replication or by mutagens (chemicals, temperature, UV light, radiation) Mutations change the meaning of genes. Types of Mutations. Point mutations Base substitution Base deletion

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Genetics and Heredity II

Genetics and Heredity II. Complete Dominance. The dominant allele completely masks the recessive allele in the heterozygous condition Example: RR = red Rr = red rr = white. Complete Dominance.

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PRESENTATION ON

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Hemophilia

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Genetic Disorders

Genetic Disorders. Cystic Fibrosis. Cystic Fibrosis. Sickle Cell Anemia. Sickle Cell Anemia. Hemophilia. Hemophilia. Tay Sachs Disease. Tay Sachs Disease. Every person of Jewish, Irish, or French- Canadian heritage is advised to be tested.

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Hemophilia

Hemophilia. David Ziga & Ryan Ehlers. What is Hemophilia?. Hemophilia is caused by an abnormal gene causing bleeding in the joints. Hemophilia slows down the blood clotting process and causes prolonged bleeding after injury . Symtoms.

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Hemophilia

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Ch5 Sec2

Ch5 Sec2. Human Genetic Disorders. Key Concepts. What are two major causes of genetic disorders in humans? How do geneticists trace the inheritance of traits? How are genetic disorders diagnosed and treated?. Key Terms. Genetic disorder Pedigree Karyotype. Ch5 Sec2.

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Hemophilia ??? Drug Pipeline Analysis and Market to 2016

The Hemophilia Therapeutics Market is Forecast to Show Slow Growth to 2016

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