Literature DB >> 29037749

Psychopathological features in Noonan syndrome.

Francesca Perrino1, Serena Licchelli2, Giulia Serra3, Giorgia Piccini2, Cristina Caciolo2, Patrizio Pasqualetti4, Flavia Cirillo2, Chiara Leoni1, Maria Cristina Digilio5, Giuseppe Zampino1, Marco Tartaglia5, Paolo Alfieri6, Stefano Vicari2.   

Abstract

INTRODUCTION: Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, skeletal and haematological/lymphatic defects, distinctive facies, cryptorchidism, and a wide spectrum of congenital heart defects. Recurrent features also include variable cognitive deficits and behavioural problems. Recent research has been focused on the assessment of prevalence, age of onset and characterization of psychiatric features in this disorder. Herein, we evaluated the prevalence of attention deficit and hyperactivity disorder (ADHD), anxiety and depressive symptoms and syndromes in a cohort of individuals with clinical and molecular diagnosis of NS.
METHODS: The Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children Present and Lifetime version (K-SADS PL) has been used for the assessment of psychiatric disorders according to Diagnostic and Statistical Manual of Mental Disorders (DSM-IV). Multidimensional Anxiety Scale for Children (MASC) and the Children's Depression Inventory (CDI) have been assessed for the evaluation of anxiety and depressive symptoms and syndromes, whereas Conners Teacher and Parent Rating Scales-long version (CRS-R) have been used to evaluate ADHD.
RESULTS: The study included 27 individuals (67% males) with an average age of 10.4 years (range 6-18 years) receiving molecular diagnosis of NS or a clinically related condition, evaluated and treated at the Neuropsychiatric Unit of Children's Hospital Bambino Gesù and at the Center for Rare Diseases of Fondazione Policlinico Universitario Agostino Gemelli, in Rome. Twenty individuals showed mutations in PTPN11, five in SOS1 and two in SHOC2. The mean IQ was 94 (Standard Deviation = 17, min = 56, max = 130). Seventy percent of the individuals (n = 19; 95% Confidence Interval = 52-85%) showed ADHD features, with six individuals reaching DSM-IV-TR criteria for ADHD disorder, and thirteen showing subsyndromal traits. Symptoms or syndrome of anxiety were present in 37% of the cohort (n = 10; 95% Confidence Interval = 19-56%), with two individuals showing anxiety disorder and eight cases exhibiting subsyndromal traits.
CONCLUSION: Our results show individuals with NS do present a very high risk to develop psychiatric disorders or symptoms during paediatric age. Based on these findings, preschool assessment of inattentive, hyperactivity/impulsivity and anxiety/depressive symptoms is recommended in order to plan a personalized treatment for psychological/psychiatric issues in affected individuals. Dedicated prospective studies are required to confirm the present data and better characterize the psychopathological profile in NS.
Copyright © 2017 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  ADHD; Anxiety; Behavioural phenotype; Depression; Noonan syndrome

Mesh:

Year:  2017        PMID: 29037749     DOI: 10.1016/j.ejpn.2017.09.009

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  8 in total

1.  PTPN11 Gain-of-Function Mutations Affect the Developing Human Brain, Memory, and Attention.

Authors:  Emily M Johnson; Alexandra D Ishak; Paige E Naylor; David A Stevenson; Allan L Reiss; Tamar Green
Journal:  Cereb Cortex       Date:  2019-07-05       Impact factor: 5.357

Review 2.  Multidisciplinary Management of Costello Syndrome: Current Perspectives.

Authors:  Chiara Leoni; Germana Viscogliosi; Marco Tartaglia; Yoko Aoki; Giuseppe Zampino
Journal:  J Multidiscip Healthc       Date:  2022-06-02

3.  Recognition Memory in Noonan Syndrome.

Authors:  Floriana Costanzo; Paolo Alfieri; Cristina Caciolo; Paola Bergonzini; Francesca Perrino; Giuseppe Zampino; Chiara Leoni; Deny Menghini; Maria Cristina Digilio; Marco Tartaglia; Stefano Vicari; Giovanni Augusto Carlesimo
Journal:  Brain Sci       Date:  2021-01-29

4.  Social skills in children with RASopathies: a comparison of Noonan syndrome and neurofibromatosis type 1.

Authors:  Elizabeth I Pierpont; Rebekah L Hudock; Allison M Foy; Margaret Semrud-Clikeman; Mary Ella Pierpont; Susan A Berry; Ryan Shanley; Nathan Rubin; Katherine Sommer; Christopher L Moertel
Journal:  J Neurodev Disord       Date:  2018-06-18       Impact factor: 4.025

5.  Defining language disorders in children and adolescents with Noonan Syndrome.

Authors:  Giulia Lazzaro; Cristina Caciolo; Deny Menghini; Francesca Cumbo; Maria C Digilio; Rossella Capolino; Giuseppe Zampino; Marco Tartaglia; Stefano Vicari; Paolo Alfieri
Journal:  Mol Genet Genomic Med       Date:  2020-02-14       Impact factor: 2.183

6.  Personality and Psychopathology in Adults with Noonan Syndrome.

Authors:  Renée L Roelofs; Ellen Wingbermühle; Paul T van der Heijden; Rosella Jonkers; Marieke de Haan; Roy P C Kessels; Jos I M Egger
Journal:  J Clin Psychol Med Settings       Date:  2020-06

7.  Social behavior in RASopathies and idiopathic autism.

Authors:  Allison M H Foy; Rebekah L Hudock; Ryan Shanley; Elizabeth I Pierpont
Journal:  J Neurodev Disord       Date:  2022-01-12       Impact factor: 4.025

8.  Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene Variants.

Authors:  Ellen Wingbermühle; Renée L Roelofs; Wouter Oomens; Jennifer Kramer; Jos M T Draaisma; Erika Leenders; Tjitske Kleefstra; Roy P C Kessels; Jos I M Egger
Journal:  J Clin Med       Date:  2022-08-13       Impact factor: 4.964

  8 in total

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