Jackson Friesth Period 5 Biology. The Origin of Muscular Dystrophy Muscular dystrophy is a recessive gene, that if passed down will cripple vital muscle.

Slides:



Advertisements
Similar presentations
Muscular Dystrophy Kate DeAngelis AP Biology 1/6/09 Kate DeAngelis AP Biology 1/6/09 Charles DeAngelis:
Advertisements

HEMOPHILIA By: Jess Gardner and Claire Griffin.
Sara Kline Period 6 3/25/10. What is Alport Syndrome?  Chromosomal disorder that damages tiny blood vessels in the kidneys - - these tiny blood vessels.
Sex Linked Genes The Xs and Ys of Genetics. Sex Linked Genes There are 23 pairs of chromosomes and one of those pairs are the sex chromosomes. There are.
NOTES 24 – Genetic Disorders and Hereditary Diseases
Duchenne Muscular Dystrophy
MUSCULAR DYSTROPHY By Jasmine DeLong. INHERITANCE Muscular dystrophy is a hereditary condition marked by progressive weakening and wasting of the muscles.
By: Amber Elizabeth McVaugh
What’s Your Blood Type? A B AB O.
Unit 4 Genetics Ch. 14 The Human Genome.
By: Isabelle Masloski and Will Michels Period 4.  Muscular Dystrophy is an inherited disorder where your muscles weaken and tissue is loss.  It continually.
Duchenne Muscular Dystrophy
Fragile x syndrome By Jordon Nagel.
 Genes are found on the X AND Y chromosomes.  Genes that are carried on the sex chromosomes are called sex linked genes.
Duchenne Muscular Dystrophy (DMD) Thomas Cooper English 2010 Professor Weatbrook.
Commonly referred to as DMD The disease was first described by the Neapolitan physician Giovanni Semmola in 1834 and Gaetano Conte in 1836 DMD is named.
List at least 3 genetic conditions you know of. Why do you think they are genetic conditions?
INHERITED GENETIC DISORDERS
IN Today we will be studying several common genetic disorders inherited by humans. How do you think a FAMILY is impacted when a child in the family is.
Chapter 14 – The Human Genome
Tristan Zvolensky p.4 December 1st, 2014
By: Logan Gillings, Reyes E. Cause Of Disease  Is a genetic disorder that causes progressive muscle weakness as individual muscle cells die.  An absence.
M USCULAR D YSTROPHY By: Collin Lowe. C AUSES Muscular Dystrophy is inherited in an X-linked recessive pattern, meaning that the mutated gene that causes.
Phenylketonuria (PKU) By: Greg Ancmon and Brennan Ramos Period 2.
(DMD) Duchenne Muscular Dystrophy. History of DMD It was first described by a french neurologist named Guillaume Benjamin Amand Duchenne in Previous.
Haemophilia The bleeding disorder. Amna Ghazali. The Nature of Haemophilia Haemophilia is a hereditary disorder; meaning people are affected from birth.
ABO Blood Groups and Genetic Disorders
What is hemophilia and how is it passed on?
OF THE MUSCULAR SYSTEM Diseases and Disorders. Anabolic Steroids Anabolic steroids are man-made substances related to male sex hormones. Medical uses.
Duchenne Muscular Dystrophy Jared Rubenstein. What Causes DMD? Caused by a mutation in a gene, called the DMD gene that can be inherited in families in.
Muscular Dystrophy. The Defect Muscular dystrophy is a group of inherited disorders that involve muscle weakness and loss of muscle tissue, which get.
Skeletal and Muscular. Brittni Parrish..
Sex Determination Sex determined by genes found on the X and Y chromosome Females: egg produced with an X chromosome Males: ½ sperm cells contain X;
Genetics Hemophilia Presentation By Will Mcauliffe-Trefz-Genetics.
Chapter 12.7 Examples of X-Linked Inheritance Patterns AP Biology Fall 2010.
CHAPTER 9 Patterns of Inheritance Part 3. Human Genetic Analysis  Since humans live under variable conditions, in different places, and have long life.
DISEASE ASSOCIATED WITH MUSCLES IN CHILDHOOD MUSCULAR DYSTROPHY.
Sex Linked Genes The Xs and Ys of Genetics. Sex Linked Genes There are 23 pairs of chromosomes and one of those pairs are the sex chromosomes. There are.
Date:01 December 2015 Time:6:30 – 9:30 pm Location:Emory University Presentation Room 308 Speakers:Dr. John Richardson National DMD Assoc. President Got.
Biology 7.4 and 7.5.
Sex-Linked Traits. The X and Y chromosomes determine gender, but they also carry other traits. These traits are called sex-linked. If the gene is on the.
Duchenne Muscular Dystrophy By: Andrea Ortega. Chromosome Graphic.
Hemophilia By: Maya Kolakowski. What is Hemophilia? Hemophilia is a group of hereditary genetic disorders that impair the body's ability to control blood.
DYSTROPHY MUSCULAR Isamar Villacrés Carlos Carlosama.
Huntington’s Disease Facts & Information By Matthew Cannon.
Duchenne Muscular Dystrophy By: Callia Ricozzi. What is Muscular Dystrophy?  The deterioration of the muscles  Dystrophin not made  gene mutation 
Sex Linked Inheritance
Duchenne's Muscular Dystrophy By: Timothy Taggart & Mark Miville-Deschenes.
What is muscular dystrophy? The muscular dystrophies (MD) are a group of genetic diseases characterized by progressive weakness and degeneration of the.
Tay-Sachs disease By Marco Rabello July/2005 NS 215 Dr.Williams.
Genetics and its relation to neuromuscular diseases
Inheritance Lesson 5.
ABO Blood Groups and Genetic Disorders
Somatic Cells – aka Body Cells
October 30, 2015 TO DO: Notebook, pencil/pen WARM UP: HOMEWORK:
Human Genetics.
The Xs and Ys of Genetics
INHERITED GENETIC DISORDERS
Chromosomes, Autosomes and Sex chromosomes
Sex linked Inheritance
The Xs and Ys of Genetics
X-linked inheritance Oliver Quarrell.
Genetics of sex Women & men are very different, but just a few genes create that difference In mammals = 2 sex chromosomes X & Y 2 X chromosomes = female:
The family tree of genetics
Duchenne’s muscular dystrophy
Sex Linked Inheritance
The family tree of genetics
The Xs and Ys of Genetics
Presentation transcript:

Jackson Friesth Period 5 Biology

The Origin of Muscular Dystrophy Muscular dystrophy is a recessive gene, that if passed down will cripple vital muscle tissue that is essential for human movement. MD is also an X linked recessive trait, meaning that males are more affected by the disease because they only have one X chromosome so they only need one faulty gene to be present instead of two required for women. The cause for Duchenne/Becker Muscular Dystrophy is due to an altered DMD gene which is responsible for making the protein dystrophin, which is believed this protein helps protect and stabilize muscle tissue.

Muscular Dystrophy Facts: There is no current treatment for MD. However people can go through physical therapy to improve muscle mobility. Muscular Dystrophy affects 1 in 3,000 newborn males. Females are rarely affected by Duchenne/Becker Muscular Dystrophy due to their decreased chances of receiving two of the same X-traits. There are around 250,000 cases in the US alone. The diagnosis of muscular dystrophy is based on the results of a muscle biopsy and increased creatine phosphokinase. In some cases, a DNA blood test may be all that is needed. A son of a carrier of MD has around a fifty percent chance of developing the disease, while a daughter of a carrier has a fifty percent chance of becoming only a carrier of the disease, which means she will never actually develop the disease but will still have the ability to pass it on to her children.

Facts Continued Symptoms include (but are not limited to): Progressive muscular wasting, poor balance, drooping eyelids, Gonadal, loss of bladder The severity of the disease is “case by case” but there is a wide age range as far as who may experience the symptoms of the disease Stem Cell research is currently being used to regenerate damaged tissue and could potentially even cure the disease if the technology is further developed.

Life With Muscular Dystrophy Life with MD varies on how severe and what type of MD they have. Many types of MD are mild and slowly become worse over time. However, other types tend to be more severe and can result in paralysis or even death. Someone with MD may have limited mobility and often can not speak efficiently. It is generally hard for a patient to get around often will require lifetime assistance (a nurse or wheelchair)

Possibility Of A Cure! Although there is no current technology to combat the effects of MD, a Cure for the disease is very probable and most likely under construction with stem cell research. However with MD being a genetic trait passed down and carried by many people throughout the world it would be difficult to determine who actually had the disease (especially in women. The technology is practical, and there may be a day in the near future where MD is driven to extinction.

Bibliography trophy.aspx trophy.aspx