Title of article
Duchenne muscular dystophy: A short review and treatment update
Author/Authors
topaloglu, haluk yeditepe university - department of pediatrics, istanbul, Turkey
From page
9
To page
15
Abstract
After advances in clinical care and newer efforts in therapeutic approaches, life span has lengthened in Duchenne muscular dystrophy (DMD). Starting from eary 1980s, each decade lead to a five year gain. DMD is not simply a monogenic X-linked disorder, it is a multisystemic condition. Pulmonary, cardiac, endocrine, gastrointestinal, and bone health aspects need careful monitoring along with pyschology, physiotherapy, social and family as a whole. Molecular treatments are becoming facts, which some are already at hand. Some others are expected to be available within the next two years.
Keywords
Duchenne muscular dystrophy , Clinical care , Newer treatments
Journal title
Iranian Journal of Child Neurology (IJCN)
Journal title
Iranian Journal of Child Neurology (IJCN)
Record number
2669287
Link To Document