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Objective: To describe the clinical and molecular genetic findings in 2 carriers of Duchenne muscular dystrophy (DMD) who exhibited marked hemiatrophy. Duchenne muscular dystrophy is an X-linked disorder in which affected male patients harbor mutations in the dystrophin gene. Female patients with heterozygous mutations may be manifesting carriers. Design: Case study. Setting: Neurology clinic. Patients: Two manifesting carriers of DMD. Interventions: Clinical and radiologic examinations alongdoi:10.1001/archneurol.2010.58 pmid:20385919 fatcat:eoveat5tgncgvnl2ljbfedzhy4