Estudio descriptivo del perfil neuropsicológico y psicopatológico en pacientes con distrofia miotónica tipo 1

Seijas-Gómez, Raquel; Basterra-Jimenez, Izaskun; Luna-Lario, Pilar; Tirapu-Ustárroz, Javier; Cabada-Giadas, Teresa; Iridoy-Zulet, Marina; Jericó-Pascual, Ivonne; Gargallo-Vaamonde, Álvaro; López-Goñi, José Javier

doi:10.33588/rn.6112.2015299

Cited by 3 publications

(3 citation statements)

References 40 publications

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“…Aunque los problemas psiquiátricos no suelen ser graves, la depresión mayor y las alteraciones de la personalidad confieren a los pacientes con DM1 unas características psicológicas especiales 34 . Es frecuente que muestren rasgos de trastorno esquizoide, ansiedad, histeria, compulsión, neurosis depresiva, carácter autodestructivo o narcisista, falta de iniciativa y apatía 24,35,36 .…”

Section: Depresión Y Trastornos De La Personalidadunclassified

“…Así, durante el parto, las mujeres presentan contracciones uterinas inadecuadas, retraso en la relajación uterina y aumento del trabajo de parto. Tras el parto existe un mayor riesgo de hemorragia y de retención de la placenta por incompetencia muscular uterina 34 .…”

Section: Sistema Genitourinariounclassified

“…La vejiga de los pacientes con DM1 suele ser normal, y ocasionalmente pueden encontrarse dilataciones focales en los uréteres 34 .…”

Section: Sistema Genitourinariounclassified

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Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert

et al. 2019

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Section: Depresión Y Trastornos De La Personalidadunclassified

Section: Sistema Genitourinariounclassified

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Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert

et al. 2019

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Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease

Gutiérrez-Gutiérrez

Díaz‐Manera

Almendrote

et al. 2019

Medicina Clínica (English Edition)

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A meta-analysis of the prevalence of neuropsychiatric disorders and their association with disease onset in myotonic dystrophy

Pascual-Morena,

Martínez-Vizcaíno,

Cavero-Redondo

et al. 2024

Acta Neuropsychiatr.

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There is a high prevalence of neuropsychiatric disorders in myotonic dystrophy types 1 and 2 (DM1 and DM2), including autism spectrum disorder (ASD) and attention deficit hyperactivity disorder (ADHD) in DM1, and depression and anxiety in both DMs. The aim of this systematic review and meta-analysis was to estimate the prevalence of ASD, ADHD, depression and anxiety in the population with DM, and their association with disease onset. A systematic search of Medline, Scopus, Web of Science, and the Cochrane Library was conducted from inception to November 2023. Observational studies estimating the prevalence of these disorders in DM1 or DM2 were included. A meta-analysis of the prevalence of these disorders and an association study with disease onset by prevalence ratio meta-analysis were performed. Thirty-eight studies were included. In DM1, the prevalence of ASD was 14%, with congenital onset being 79% more common than juvenile onset, while the prevalence of ADHD was 21%, with no difference between congenital and juvenile onset, and the prevalence of depression and anxiety were 14% and 16%. Depression was more common in the adult onset. Finally, the prevalence of depression in DM2 was 16%. A higher prevalence of neuropsychiatric disorders is observed in individuals with DM1 and DM2 than in the general population. Therefore, actively screening for congenital and juvenile neurodevelopmental disorders in DM1 and emotional disorders in DM1 and DM2 may improve the quality of life of those affected.

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Estudio descriptivo del perfil neuropsicológico y psicopatológico en pacientes con distrofia miotónica tipo 1

Cited by 3 publications

References 40 publications

Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert

Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease

A meta-analysis of the prevalence of neuropsychiatric disorders and their association with disease onset in myotonic dystrophy

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