Nnnparalisis de duchenne pdf

Duchenne muscular dystrophy duchenne muscular dystrophy dmd is a common disorder affecting the muscular system. Scribd is the worlds largest social reading and publishing site. This form of muscular dystrophy is inherited and is caused by a genetic mutation that affects the dystrophin proteins of the muscles. Abuchamneto 2, mariza polati 2, gerson chadi 1,umbertina c. Creatine monohydrate in duchenne muscular dystrophy. Essay on duchenne muscular dystrophy 18 words cram. Duchenne spierdystrofie is een xgebonden recessieve spierziekte met een progressief beloop. The dystrophinopathies cover a spectrum of xlinked muscle disease ranging from mild to severe that includes duchenne muscular dystrophy, becker muscular dystrophy, and dmdassociated dilated cardiomyopathy dcm. Discourses of aesthetics, sexuality, and power in nineteenthcentury medical photography hayes peter mauro the work of dr. Ook bij jongens met duchenne komt zie verder pdfdocument. Duchenne muscular dystrophy dmd is a genetic condition which affects the muscles, causing muscle weakness. Owing to the lack of the dystrophin protein, muscle fibres break down and are replaced by fibrous and or fatty tissue causing the muscle to weaken gradually. The diagnosis and management of duchenne muscular dystrophy, part 2.

It causes fatigue and progressive muscle weakness, eventually resulting in loss of ambulation and respiratory compromise. Duchenne muscular dystrophy is a serious condition that causes progressive muscle weakness. Erbduchenne et dejerineklumpke sont des paralysies du plexus brachial. Spurney, md division of cardiology, research center for genetic medicine, childrens national medical center, 111 michigan avenue nw, washington, dc 20010, usa accepted 7 march 2011 abstract. The muscle weakness is not noticeable at birth, even though the child is born with the gene which causes it. Creatine monohydrate in duchenne muscular dystrophy duchenne muscular dystrophy dmd is one of the most common muscle diseases, affecting around 1 in 3500 boys 1. The mild end of the spectrum includes the phenotypes of asymptomatic increase in serum concentration of creatine phosphokinase ck and muscle. Duchenne, a french physiologist and psychiatrist, conducted a series. It is a serious condition which starts in early childhood. Bij kinderen zonder duchenne maar met obesitas wordt een lagere botdichtheid gezien. The weakness develops gradually, usually noticeable by the age of three. Duchenne spierdystrofie nieuws per diagnose documenten. Bij duchenne spierdystrofie, een ernstige spierziekte, worden meestal deleties dat wil zeggen.