'Tay sachs disease' diaporamas de présentation

HUMAN GENETICS

1.26k views • 104 slides

Inborn Errors of Metabolism

Inborn Errors of Metabolism. Dr B.Vahabi. Lecture outcomes. Understand the general pathophysiology underlying the inborn errors of metabolism (IEMs) Review some important IEMs Understand the genetic inheritance of IEMs Review the general diagnostic methods used for detection of IEMs

744 views • 56 slides

Human Genetics: Genetic Disorders

717 views • 55 slides

Organelles of Eukaryotic Cells

Organelles of Eukaryotic Cells. AHMP 5406. Objectives. List the principle functions and describe the structure of the nucleus, mitochondrion, endoplasmic reticulum, Golgi, lysosomes and peroxisomes in higher eukaryotes

1.04k views • 51 slides

NEURODEGENERATIVE DISORDERS OF CHILDHOOD

NEURODEGENERATIVE DISORDERS OF CHILDHOOD. Neurodegenerative disorders of childhood. A group of heterogenous diseases resulting from Genetic and biochemical defects Chronic viral infection Toxic substances Unknown cause. Neurodegenerative disorders of childhood.

958 views • 51 slides

CHAPTER 9 Patterns of Inheritance

452 views • 44 slides

CHAPTER 9 Patterns of Inheritance

667 views • 43 slides

Do Now

Do Now. Explain the difference between transcription and translation. (Hint: Think about what is made) Explain difference between codon and anticodon . 3. After answering the above questions get out a piece of scratch paper. What is the protein for the DNA strand below?.

643 views • 33 slides

Chapter 20

Chapter 20. Patterns of Genetic Inheritance. Points to Ponder. What is the genotype and the phenotype of an individual? What are the genotypes for a homozygous recessive and dominant individuals and a heterozygote individual?

409 views • 33 slides

Chapter 20

Chapter 20. Patterns of Genetic Inheritance. Points to Ponder. What is the genotype and the phenotype of an individual? What are the genotypes for a homozygous recessive and dominant individuals and a heterozygote individual?

393 views • 33 slides

544 views • 31 slides

Chapter 4 Notes

352 views • 29 slides

Tay-sachs-Disease

Tay-sachs-Disease. By: Cory Hawkins & Tj Cartwright. Tay-Sachs- Disease. Where harmful quantities of ganglioside builds up Causes infants to die at an early age People show no sign. Pedigree of disease. What causes tay-sachs-disease?. Mutations in the HEX A causes TSD

351 views • 11 slides

111 views • 11 slides

113 views • 11 slides

Tay -Sachs Disease

546 views • 10 slides

Tay-Sachs Disease

317 views • 10 slides

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.

299 views • 9 slides

Tay Sachs Disease

Tay Sachs Disease. By: Jonathan Cookmeyer and Mehran Hazheer. Cause. Chromosome 15 Protein hexosaminidase A (HEX A) GM2 gangliosides. Symptoms. Red spot retina Motor/metal skills Paralysis Cramps Slurred speech Behavioral changes. Treatment. None for Early/Juvenile

213 views • 7 slides

10 Second Case Studies

10 Second Case Studies. Round 2: Degenerative Neurological Conditions. PATIENT 1. 55 years old male Lateralized left-side muscle weakness Dysphagia (difficulty swallowing) Progressive difficulties with breathing No familial history of similar symptoms Your diagnosis?

199 views • 6 slides