genetic presentation
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Duchenne Muscular Dystrophy
(DMD)
Characteristics of the disease
The disease attacks the muscular tissue and degenerates it.
Its incidence is about 1 in 3,600 boys, girls are mostly carriers
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
DMD has an incidence of 1 in 4,000 male babies
The disease is usually inherited in the genes
With medical care the boy can live to his 30s
Treatments
There is no cure for this disease yet
Decrease muscular degenerations using steroids, to extend the life of the person.
The patient should visit the physiotherapist, and occupational therapists often, for about every 4 moths
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
The allele for this disease is located in the X chromosome
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.
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.
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
http://en.wikipedia.org/wiki/Duchenne_muscular_dystrophy#Symptoms
http://www.muscular-dystrophy.org/about_muscular_dystrophy/conditions/97_duchenne_muscular_dystrophy
http://www.muscular-dystrophy.org/about_muscular_dystrophy/conditions/97_duchenne_muscular_dystrophy
http://www.genome.gov/19518854