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Duchenne Muscular
    Dystrophy
     (DMD)




                    S
Characteristics of the disease

S   The disease attacks the muscular tissue and
    degenerates it.

S   Its incidence is about 1 in 3,600 boys, girls are mostly
    carriers

S   Some symptoms are: awkward walking, fatigue,
    frequent falls, difficulties with motor skill, and
    difficulties while breading, this symptoms usually
    appear at the age of 5 in males

S   DMD has an incidence of 1 in 4,000 male babies

S   The disease is usually inherited in the genes

S   With medical care the boy can live to his 30s
S There is no cure for this
              disease yet
Treatment   S Decrease muscular
s             degenerations using
              steroids, to extend the
              life of the person.
            S The patient should visit
              the physiotherapist, and
              occupational therapists
              often, for about every 4
              moths
            S And visit your doctor for
              about every 6 moths, so
              that they can make
              decisions for the
              treatment theyare going
              to apply.
Genetic Part of DMD

S   The allele for this disease is located in the X
    chromosome

S   This disease is most likely to be inherited by
    males rather than females, because for the
    male if the allele is present in X chromosome
    he is affected, but girls have to have the
    allele present in each X chromosome.

S   Its is most like like that the boy has a 50, 50
    change of be affected with a the disease or
    not and girls have a 50 ,50 change of either
    caring the disease or not accruing it.

S   This disease is a sex-linked recessive
    disease ,because some of the girls carry this
    allele as recessive and later can be brought
    by her and his children
Bibliography


S   http://en.wikipedia.org/wiki/Duchenne_muscular_dystrophy#Symptoms

S   http://www.muscular-
    dystrophy.org/about_muscular_dystrophy/conditions/97_duchenne_musc
    ular_dystrophy

S   http://www.muscular-
    dystrophy.org/about_muscular_dystrophy/conditions/97_duchenne_musc
    ular_dystrophy

S   http://www.genome.gov/19518854

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Genetic presentation

  • 1. Duchenne Muscular Dystrophy (DMD) S
  • 2. Characteristics of the disease S The disease attacks the muscular tissue and degenerates it. S Its incidence is about 1 in 3,600 boys, girls are mostly carriers S Some symptoms are: awkward walking, fatigue, frequent falls, difficulties with motor skill, and difficulties while breading, this symptoms usually appear at the age of 5 in males S DMD has an incidence of 1 in 4,000 male babies S The disease is usually inherited in the genes S With medical care the boy can live to his 30s
  • 3. S There is no cure for this disease yet Treatment S Decrease muscular s degenerations using steroids, to extend the life of the person. S The patient should visit the physiotherapist, and occupational therapists often, for about every 4 moths S And visit your doctor for about every 6 moths, so that they can make decisions for the treatment theyare going to apply.
  • 4. Genetic Part of DMD S The allele for this disease is located in the X chromosome S This disease is most likely to be inherited by males rather than females, because for the male if the allele is present in X chromosome he is affected, but girls have to have the allele present in each X chromosome. S Its is most like like that the boy has a 50, 50 change of be affected with a the disease or not and girls have a 50 ,50 change of either caring the disease or not accruing it. S This disease is a sex-linked recessive disease ,because some of the girls carry this allele as recessive and later can be brought by her and his children
  • 5. Bibliography S http://en.wikipedia.org/wiki/Duchenne_muscular_dystrophy#Symptoms S http://www.muscular- dystrophy.org/about_muscular_dystrophy/conditions/97_duchenne_musc ular_dystrophy S http://www.muscular- dystrophy.org/about_muscular_dystrophy/conditions/97_duchenne_musc ular_dystrophy S http://www.genome.gov/19518854