Diagnostic and clinical characteristics of early-manifesting females with Duchenne or Becker muscular dystrophy
Author:
Affiliation:
1. Department of Pediatrics; the University of Arizona College of Medicine; Tucson Arizona
2. Department of Neurology; University of Rochester; Rochester New York
Funder
Centers for Disease Control and Prevention
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Cardiovascular health supervision for individuals affected by Duchenne or Becker muscular dystrophy;American Academy of Pediatrics Section on Cardiology and Cardiac Surgery;Pediatrics,2005
2. Prevalence of autism spectrum disorders-Autism and developmental disabilities monitoring network, 14 sites, United States, 2008;CDC;MMWR,2012
3. Delayed diagnosis in Duchenne muscular dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet);Ciafaloni;J Pediatr,2009
4. Survey of behaviour problems in children with neuromuscular diseases;Darke;J Child Neurol,2006
5. Inheritance of most X-linked traits is not dominant or recessive, just X-linked;Dobyns;Am J Med Genet A,2004
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1. Preventing Progressivity in Becker Muscular Dystrophy Patient: A Rare Case Report;Indonesian Journal of Physical Medicine and Rehabilitation;2024-06-27
2. Long‐term outcomes for females with early‐onset dystrophinopathy;Developmental Medicine & Child Neurology;2022-12-23
3. Dystrophinopathies;Česko-slovenská pediatrie;2022-08-25
4. Cognitive profile and neuropsychiatric disorders in Becker muscular dystrophy: A systematic review of literature;Neuroscience & Biobehavioral Reviews;2022-06
5. Dystrophin genetic variants and autism;Discover Mental Health;2022-03-24
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