학술논문

Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy
Document Type
TEXT
Source
European Child & Adolescent Psychiatry, 18(12)
European Child & Adolescent Psychiatry, 18 (12)
Subject
Medizin und Gesundheit
Psychologie
Medizin, Sozialmedizin
psychische Störungen, Behandlung und Prävention
Psychology
Medicine and health
Myotonic dystrophy type 1; Juvenile form; Psychiatric phenotype; Cognitive profile
Psychological Disorders, Mental Health Treatment and Prevention
Medicine, Social Medicine
Language
English
Abstract
Myotonic dystrophy type 1 (DM1) is the most frequent inherited neuromuscular disorder. The juvenile form has been associated with cognitive and psychiatric dysfunction, but the phenotype remains unclear. We reviewed the literature to examine the psychiatric phenotype of juvenile DM1 and performed an admixture analysis of the IQ distribution of our own patients, as we hypothesised a bimodal distribution. Two-thirds of the patients had at least one DSM-IV diagnosis, mainly attention deficit/ hyperactivity disorder and anxiety disorder. Two-thirds had learning disabilities comorbid with mental retardation on one hand, but also attention deficit, low cognitive speed and visual spatial impairment on the other. IQ showed a bi-modal distribution and was associated with parental transmission. The psychiatric phenotype in juvenile DM1 is complex. We distinguished two different phenotypic subtypes: one group characterised by mental retardation, severe developmental delay and maternal transmission; and another group characterised by borderline full scale IQ, subnormal development and paternal transmission.