Abstract: A diagnosis of autism spectrum disorder is reported in up to 19% of dystrophinopathies. However, over the last ten years, only a few papers have been published on this topic. Therefore, further studies are required to analyze this association in depth and ultimately to understand the role of the brain dystrophin isoform in the pathogenesis of ASD and other neurodevelopmental disorders. In this paper, we report a clinical case of a patient affected by ASD and Duchenne muscular dystrophy, who carries a large deletion of the dystrophin gene. Then we present a brief overview of the literature about similar cases and about the potential role of the dystrophin protein in the neurobiology of autism spectrum disord
Dystrophinopaties, e.g., Duchenne muscular dystrophy (DMD), Becker muscular dystrophy and X-linked d...
Duchenne muscular dystrophy is a multifactorial disease including a cognitive phenotype. It is cause...
Duchenne muscular dystrophy (DMD) is a recessive hereditary form of muscular dystrophy caused by a m...
Abstract: A diagnosis of autism spectrum disorder is reported in up to 19% of dystrophinopathies. H...
social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne...
Intelligence of individuals with Duchenne muscular dystrophy (DMD) is lower than the general populat...
O Transtorno do Espectro do Autismo (TEA) compreende um quadro complexo do neurodesenvolvimento acom...
BACKGROUND: Duchenne muscular dystrophy (DMD) is the most frequent and severe form of the dystrophin...
Objective Duchenne Muscular Dystrophy (DMD) is a progressive neuromuscular condition that has a hig...
Background: Individuals with Duchenne muscular dystrophy (DMD) often have lower intelligence than t...
Functional Genomics of Muscle, Nerve and Brain DisordersMolecular Technology and Informatics for Per...
AbstractThe presence of nonprogressive cognitive impairment is recognized as a common feature in a s...
Muscular dystrophies have historically been characterised according to clinical criteria, however in...
Aim: Duchenne muscular dystrophy (DMD) is associated with neuropsychiatric disorders. The aim of the...
International audienceMutations of the dystrophin DMD gene, essentially deletions of one or several ...
Dystrophinopaties, e.g., Duchenne muscular dystrophy (DMD), Becker muscular dystrophy and X-linked d...
Duchenne muscular dystrophy is a multifactorial disease including a cognitive phenotype. It is cause...
Duchenne muscular dystrophy (DMD) is a recessive hereditary form of muscular dystrophy caused by a m...
Abstract: A diagnosis of autism spectrum disorder is reported in up to 19% of dystrophinopathies. H...
social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne...
Intelligence of individuals with Duchenne muscular dystrophy (DMD) is lower than the general populat...
O Transtorno do Espectro do Autismo (TEA) compreende um quadro complexo do neurodesenvolvimento acom...
BACKGROUND: Duchenne muscular dystrophy (DMD) is the most frequent and severe form of the dystrophin...
Objective Duchenne Muscular Dystrophy (DMD) is a progressive neuromuscular condition that has a hig...
Background: Individuals with Duchenne muscular dystrophy (DMD) often have lower intelligence than t...
Functional Genomics of Muscle, Nerve and Brain DisordersMolecular Technology and Informatics for Per...
AbstractThe presence of nonprogressive cognitive impairment is recognized as a common feature in a s...
Muscular dystrophies have historically been characterised according to clinical criteria, however in...
Aim: Duchenne muscular dystrophy (DMD) is associated with neuropsychiatric disorders. The aim of the...
International audienceMutations of the dystrophin DMD gene, essentially deletions of one or several ...
Dystrophinopaties, e.g., Duchenne muscular dystrophy (DMD), Becker muscular dystrophy and X-linked d...
Duchenne muscular dystrophy is a multifactorial disease including a cognitive phenotype. It is cause...
Duchenne muscular dystrophy (DMD) is a recessive hereditary form of muscular dystrophy caused by a m...