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Neurodevelopmental, behavioral, and emotional symptoms in Becker muscular dystrophy.
Lambert, Joshua T; Darmahkasih, Andrew J; Horn, Paul S; Rybalsky, Irina; Shellenbarger, Karen C; Tian, Cuixia; Wong, Brenda L.
Afiliação
  • Lambert JT; Neurology Division, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Darmahkasih AJ; Pediatric Residency Program, University of California-Irvine/Children's Hospital of Orange County, Orange, California.
  • Horn PS; Division of Neurology, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio.
  • Rybalsky I; Neurology Division, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Shellenbarger KC; Department of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts.
  • Tian C; Division of Neurology, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio.
  • Wong BL; Department of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts.
Muscle Nerve ; 61(2): 156-162, 2020 02.
Article em En | MEDLINE | ID: mdl-31650559
ABSTRACT

INTRODUCTION:

Becker muscular dystrophy (BMD) results in decreased dystrophin with implications for mental health.

METHODS:

This is a retrospective case series of neurodevelopmental, behavioral, and emotional symptoms and respective pharmacotherapies of 70 patients with BMD.

RESULTS:

Fifty-four (77.1%) patients exhibited at least one symptom, and 19 (27.1%) patients exhibited four or more symptoms. The most prevalent symptoms were specific learning disabilities or special education needs (31.4%), inattention/hyperactivity (35.7%), language/speech delays (35.7%), and emotional or behavioral dysregulation (38.6%). Fisher's exact tests indicated that anxiety was more prevalent with mutations upstream of exon 30 (P = .049), but the prevalence of other symptoms did not differ with respect to mutation sites. Similarly, the number of symptoms individual patients with BMD exhibited did not differ with respect to mutation sites. Seventeen (24.3%) patients required pharmacotherapy to manage symptoms.

DISCUSSION:

Neurodevelopmental, behavioral, and emotional symptoms are prevalent in patients with BMD regardless of dystrophin gene mutation site.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Distrofina / Distrofia Muscular de Duchenne / Sintomas Afetivos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Muscle Nerve Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Distrofina / Distrofia Muscular de Duchenne / Sintomas Afetivos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Muscle Nerve Ano de publicação: 2020 Tipo de documento: Article