Huntington’s Disease Facts & Information By Matthew Cannon.

Slides:



Advertisements
Similar presentations
Human Genetic Disorders
Advertisements

Medical Mystery Patient X. Symptoms 0 Patient’s Symptoms: 0 Possible Diseases/Disorders: 0 Final Diagnosis:
Huntington’s Disease By Brendan G.
Huntington’s Disease.
PRESENTATION BY: PREMED III-GROUP4 DR.GURI.T.. INTRODUCTION HISTORY DISEASE DIAGNOSIS SYMPTOMS CAUSES PREVALENCE WORLDWIDE TREATMENT AND MANAGEMENT FUTURE.
Lisa Pezik, RN BScN Clinical Educator. Discuss the physiology and incidence. Review signs and symptoms at all stages. Discuss treatment options (pharm/non-pharm).
Huntington’s Disease! Hamza Khan Jeremy Tague Period 2 January 29, 2010.
NOTES 24 – Genetic Disorders and Hereditary Diseases
Huntington’s Disease. Huntington's Disease is an autosomal dominant genetic disorder Meaning that if a parent has Huntington's there is a 50% chance the.
HUNTINGTON’S DISEASE BY ERIN DALTON WHAT IS IT? A degenerative brain disorder which currently there is no cure or effective treatment for it. Huntington’s.
Jackson Friesth Period 5 Biology. The Origin of Muscular Dystrophy Muscular dystrophy is a recessive gene, that if passed down will cripple vital muscle.
GENETIC DISORDER PROJECT EXAMPLE By: Mrs. Hoffman.
Patients present with night vision problems, which progress to a slow loss of all peripheral vision; central vision is spared the longest.
Von Recklinghausen Neurofibromatosis NF1 By: Jessica Mollman.
Gene Therapy in Huntington’s Disease Project was done by Rejan Chin & Sharisa Ford.
What is Huntington’s disease? It is a progressive degeneration of the nerve cells in the brain. This disease cause uncontrolled movements, emotional problems,
By: Kaila Cooper What is it? Huntington’s Disease s a brain disorder that affects a person’s ability to think, talk, and move.
Facts and Information on: By: Xavier Robles-Giron George Huntington.
Huntington’s Disease Michael Ou Pierce Lam.
Chromosomes and Human Inheritance  Diploid = 46, Haploid = 23  Sex chromosomes different than others  Not homologous pairs  Female = two X chromosomes.
Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.
Chapter 4, Section 2 Human Genetic Disorders
Huntington’s Disease.  A rare and incurable neurological disease that eats away at the nerves and the brain, causing total mental deterioration over.
Ataxia Telangiectasia By: Leon Richardson Period
Genetic Disorders.
You already know… - A chromosome is a structure that carries genetic information Each cell normally has 23 pairs of chromosomes: 1 pair of sex chromosomes.
Huntington’s Disease By: Ari Naccarato (Press space bar to change slides and make sure the volume is up!)
Alzheimer's Disease was named after Dr.Alois Alzheimer in 1906.
Human Heredity  This section explains what scientists know about human chromosomes, as well as the inheritance of certain human traits and disorders.
Sex-linked Genetic Disorders & Autosomal Disorders Packet #41 Chapter #14.
By: Jack Wernet.  “A gene on one of the non-sex chromosomes that is always expressed, even if only one copy is present.” (Human Genome Project Information.
Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.
CHAPTER 9 Patterns of Inheritance Part 3. Human Genetic Analysis  Since humans live under variable conditions, in different places, and have long life.
 The tics  The twitches  Usually start showing between the age of seven & ten  Males are 3 times more likely to have TS than females  Many children.
HUNTINGTON’S DISEASE MAGGIE PHOEBE LEONORA BY:. NAME OF DISORDER? ARE THERE OTHER NAMES FOR DISORDER/DISEASE (WHAT ARE THEY)? Huntington's disease -first.
Autosomal Dominance Inheritance What’s an Autosome? Autosome: Non sex chromosome – Ex: Autosomal disorders: gene for the disease is found on chromosomes.
Huntington's Disease By: Walter Gerring and Seth Little.
Huntington’s disease By Colten Appleby Kristian Nee Nick Reynoso Please check the notes section for additional information Mrs. GM Period 8 2/8/11.
Retinoblastoma. Description This disease is a cancer that affects young children. Most of the time it is caused by a mutation in the womb. It is very.
Charcot – Marie – Tooth disease
By Raivonna Moore 2/27/13 Psychology Honors Pd.4
Zookeeper genetic disorder By nick proffitt. Multiple sclerosis Multiple sclerosis also known as MS is a long lasting disease that can affect the brain.
Huntington’s Chorea Learning Objective – to know that Huntington’s is inherited via a dominant allele and the symptoms of the disease.
Hannah Beacom and Thomas Bennett Pd. 3.  Rare inherited disorder  Caused by genetic stutter  Progressive loss of nerve cells in brain  Results in.
HUNTINGTON'S DISEASE (HD) By: Jerika Adams-Harrison April 5, 2013.
Duchenne Muscular Dystrophy By: Andrea Ortega. Chromosome Graphic.
Aperts Syndrome (Acrocephalosyndactyly) By: Madison Weckerly.
HUNTINGTON’S DISEASE Neil Madadi. WHAT IS HUNTINGTON’S DISEASE?  It is an autosomal dominant inherited disease. Meaning that only one copy of the altered.
To Test, or Not to Test, That is the Question A Bioethical Project Presented by: Alla Natalie Orna IB Chemistry 4 June 2006.
Huntington’s Disease BY: SAM DAVIS, SABRINA TRAN, MYA LUNA, MYLES BLACKWELL AND EAMONN DUENSING.
Mutations – random Replication errors Don’t necessarily lead to harm, but some do Permanent change in sequence – If in gamates (sex cells), passed to offspring.
MUTATIONS 1B LIVING ENVIRONMENT MURTAUGH. ESSENTIAL QUESTIONS What is a mutation? How is gene mutation and a chromosome mutation different? Do all mutations.
Inherited Diseases © 2013 Project Lead The Way, Inc.Medical Detectives.
Retinoblastoma Retinoblastoma is a rare form of eye cancer that develops in the retina usually before the age 5.
Niemann Pick Type C Disease By: Grace Messina 11/28/15 Period 4.
Warmup 5/12/16: Turn in U8 Qualifier and signed progress report to the folder at your station Next, complete the Pedigree Review Worksheet.
Huntington’s Chorea By Alyce & Ryan.
Inherited Diseases Medical Detectives
Two copies of each autosomal gene affect phenotype.
Sex-linked Genetic Disorders & Autosomal Disorders
Kody Winget & Jenna Vandenberg
Huntington's Disease Drew Exley.
Inherited Diseases Medical Detectives
Woody Guthrie: This Land is Made for You and Me
Autosomal Dominance Inheritance
Inherited Diseases Medical Detectives
Inherited Disorders.
Inherited Diseases Medical Detectives
Huntington’s Disease Brett McCraw.
Presentation transcript:

Huntington’s Disease Facts & Information By Matthew Cannon

Cause Huntington disease is a genetics disease that is passed down in reproduction. It’s an autosomal dominant. It is on the forth autosomal chromosome on the autosomal pair. It occurs when one gene of this pair is not functioning correctly.

Characteristics Symptoms can vary significantly from person to person. Symptoms may include personality changes, decreased cognitive abilities, and uncontrolled movement. Death occurs about years after signs.

Diagnosis You can get a blood test to tell if you have Huntington’s disease. Additional tests may consist of brain scans such as CT, MRI, and EEG.

Treatment There is no treatment to stop or reverse Huntington’s but you can get medication such as Tetrabenazine to help stop symptoms. There are scientists and doctors in the village of Barranquitas in Venezuela, where there is the highest concentration of the disease.

Helpful Facts 1.It usually starts at middle age (30-50 years old) 2.Nearly one in every 10,000 people in the US are infected with Huntington’s 3.There has never been a successful case of Huntington’s cured 4.Children who develop the disease rarely live to adulthood 5.When affected you will slowly lose your ability to walk, think, talk and reason.

Here is a link on Huntington's disease

Recourses