DUCHENNE   MUSCULAR   DYSTROPHY       Foundation                       

 

Duchenne

SpierDystrofie Stichting 

Duchenne Muscular Dystrophy Foundation (Duchenne SpierDystrofie Stichting)
MOLENPAD 52
Paramaribo, -- --
Suriname

ph: (597) 483704 or (597) 08807660
fax: (597) 483704
alt: (+1) 215 290 4620 USA

FACTS  on  

DUCHENNE  MUSCULAR  DYSTROPHY

 

Dr. Guillaume-Benjamin-Amand Duchenne

Born: Sept. 17, 1806  Boulogne, France              
Died :Sept. 15, 1875  Paris France

 

Duchenne Muscular Dystrophy is named after

Dr. Duchenne of  Paris in 1861.

He is one of the first person to study Muscular Dystrophy. Duchenne Muscular Dystrophy results from a gene defect in a single important fibre in muscle fibres called dystrophin. Without dystrophin to strengthen them, the muscle cells become weaker and eventually waste away.                                                                        

 

DMD is hereditary, but some cases are caused by spontaneous mutations, which in a way is a case of

genetic roulette.                                                                                                                                       An X-linked gene causes Duchenne muscular dystrophy

(that is, the gene is on the X chromosome)

This means that only boys are affected but that their mothers may be carriers.

                                          

 

 

 

 

 

 

XX            XY

 

                    

 

 

 

 

 

 

 

GOWER  SIGN 

of DUCHENNE MD

 

Duchenne Muscular Dystrophy affects the muscles of the body, including the heart and lungs.

 

 

 

 

 

 

 

 

Duchenne Muscular Dystrophy is a very serious condition. First signs of difficulties are shown in walking, standing, climbing stairs, running, etc., between the ages of one to three years.

Between ages 8-10 children becomes wheelchair confined. Scoliosis and other medical conditions may develop due to muscle weakness.

It affects mainly boys 1 in every 2800 of any race.

 

Diagnose:

mostly by genetic tests,

CPK readings,             

Muscle biopsy,

 

Treatment:  Unfortunately until now, there is no known cure. Only different ways to manage this condition. Physical therapy, hydrotherapy, braces, steroids, support, etc.,

 

Rev. Dr. M.Singh is founder and President of the Duchenne Muscular Dystrophy Foundation in Suriname South America.

It was initiated when their son, Josia Singh, was diagnosed with the same prognosis as their

first son, Giovanni.

Josia was 3 years young when diagnosed.

On the 9th of September 2010, he will be 18 years old.   

He presented the Television program on Duchenne Muscular Dystrophy in Suriname.

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  • Muscular Dystrophy help and support group....do not give up on your child's struggle for survival.
    It's  a challenge, but take life step by step, day by day.

 

 

Copyright 2010 Duchenne Muscular Dystrophy Foundation

(Duchenne SpierDystrofie Stichting). All rights reserved.

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Duchenne Muscular Dystrophy Foundation (Duchenne SpierDystrofie Stichting)
MOLENPAD 52
Paramaribo, -- --
Suriname

ph: (597) 483704 or (597) 08807660
fax: (597) 483704
alt: (+1) 215 290 4620 USA