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Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome

Malan Syndrome (MS) is an ultra-rare overgrowth genetic syndrome due to heterozygous variants or deletions in the Nuclear Factor I X (NFIX) gene. It is characterized by an unusual facial phenotype, generalized overgrowth, intellectual disability (ID) and behavioral problems. Even though limitations...

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Autores principales: Alfieri, Paolo, Macchiaiolo, Marina, Collotta, Martina, Montanaro, Federica Alice Maria, Caciolo, Cristina, Cumbo, Francesca, Galassi, Paolo, Panfili, Filippo Maria, Cortellessa, Fabiana, Zollino, Marcella, Accadia, Maria, Seri, Marco, Tartaglia, Marco, Bartuli, Andrea, Mammì, Corrado, Vicari, Stefano, Priolo, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316998/
https://www.ncbi.nlm.nih.gov/pubmed/35887841
http://dx.doi.org/10.3390/jcm11144078
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author Alfieri, Paolo
Macchiaiolo, Marina
Collotta, Martina
Montanaro, Federica Alice Maria
Caciolo, Cristina
Cumbo, Francesca
Galassi, Paolo
Panfili, Filippo Maria
Cortellessa, Fabiana
Zollino, Marcella
Accadia, Maria
Seri, Marco
Tartaglia, Marco
Bartuli, Andrea
Mammì, Corrado
Vicari, Stefano
Priolo, Manuela
author_facet Alfieri, Paolo
Macchiaiolo, Marina
Collotta, Martina
Montanaro, Federica Alice Maria
Caciolo, Cristina
Cumbo, Francesca
Galassi, Paolo
Panfili, Filippo Maria
Cortellessa, Fabiana
Zollino, Marcella
Accadia, Maria
Seri, Marco
Tartaglia, Marco
Bartuli, Andrea
Mammì, Corrado
Vicari, Stefano
Priolo, Manuela
author_sort Alfieri, Paolo
collection PubMed
description Malan Syndrome (MS) is an ultra-rare overgrowth genetic syndrome due to heterozygous variants or deletions in the Nuclear Factor I X (NFIX) gene. It is characterized by an unusual facial phenotype, generalized overgrowth, intellectual disability (ID) and behavioral problems. Even though limitations in cognitive and adaptive functioning have been previously described, systematic studies on MS cohorts are still lacking. Here, we aim to define the cognitive and adaptive behavior profile of MS children and adolescents, providing quantitative data from standardized evaluations. Subjects included in this study were evaluated from October 2020 to January 2022 and the study is based on a retrospective data archive: fifteen MS individuals were recruited and underwent evaluation with Wechsler Intelligence Scales, Leiter International Performance Scales and Griffith Mental Development Scales for cognitive profiles and with Vineland Adaptive Behavior Scales-II Edition (VABS-II) for adaptive functioning. Language skills and visuomotor integration abilities were assessed too. Comparisons and correlations between scales and subtests were performed. All the assessed MS individuals showed both low cognitive and adaptive functioning. One subject presented with mild ID, five had moderate ID and eight showed severe ID. One female toddler received a diagnosis of psychomotor delay. Linguistic skills were impaired in all individuals, with language comprehension relatively more preserved. Results revealed significant differences between VABS-II subdomains and a strong relationship between cognitive and adaptive functioning. All subjects exhibited mild to moderate ID and adaptive behavior lower than normal, with communication skills being the most affected. Regarding the daily living skills domain, personal and community subscale scores were dramatically lower than for the domestic subdomain, highlighting the importance of considering behavior within developmental and environmental contexts. Our cognitive and adaptive MS characterization provides a more accurate quantitative MS profiling, which is expected to help clinicians to better understand the complexity of this rare disorder.
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spelling pubmed-93169982022-07-27 Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome Alfieri, Paolo Macchiaiolo, Marina Collotta, Martina Montanaro, Federica Alice Maria Caciolo, Cristina Cumbo, Francesca Galassi, Paolo Panfili, Filippo Maria Cortellessa, Fabiana Zollino, Marcella Accadia, Maria Seri, Marco Tartaglia, Marco Bartuli, Andrea Mammì, Corrado Vicari, Stefano Priolo, Manuela J Clin Med Article Malan Syndrome (MS) is an ultra-rare overgrowth genetic syndrome due to heterozygous variants or deletions in the Nuclear Factor I X (NFIX) gene. It is characterized by an unusual facial phenotype, generalized overgrowth, intellectual disability (ID) and behavioral problems. Even though limitations in cognitive and adaptive functioning have been previously described, systematic studies on MS cohorts are still lacking. Here, we aim to define the cognitive and adaptive behavior profile of MS children and adolescents, providing quantitative data from standardized evaluations. Subjects included in this study were evaluated from October 2020 to January 2022 and the study is based on a retrospective data archive: fifteen MS individuals were recruited and underwent evaluation with Wechsler Intelligence Scales, Leiter International Performance Scales and Griffith Mental Development Scales for cognitive profiles and with Vineland Adaptive Behavior Scales-II Edition (VABS-II) for adaptive functioning. Language skills and visuomotor integration abilities were assessed too. Comparisons and correlations between scales and subtests were performed. All the assessed MS individuals showed both low cognitive and adaptive functioning. One subject presented with mild ID, five had moderate ID and eight showed severe ID. One female toddler received a diagnosis of psychomotor delay. Linguistic skills were impaired in all individuals, with language comprehension relatively more preserved. Results revealed significant differences between VABS-II subdomains and a strong relationship between cognitive and adaptive functioning. All subjects exhibited mild to moderate ID and adaptive behavior lower than normal, with communication skills being the most affected. Regarding the daily living skills domain, personal and community subscale scores were dramatically lower than for the domestic subdomain, highlighting the importance of considering behavior within developmental and environmental contexts. Our cognitive and adaptive MS characterization provides a more accurate quantitative MS profiling, which is expected to help clinicians to better understand the complexity of this rare disorder. MDPI 2022-07-14 /pmc/articles/PMC9316998/ /pubmed/35887841 http://dx.doi.org/10.3390/jcm11144078 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alfieri, Paolo
Macchiaiolo, Marina
Collotta, Martina
Montanaro, Federica Alice Maria
Caciolo, Cristina
Cumbo, Francesca
Galassi, Paolo
Panfili, Filippo Maria
Cortellessa, Fabiana
Zollino, Marcella
Accadia, Maria
Seri, Marco
Tartaglia, Marco
Bartuli, Andrea
Mammì, Corrado
Vicari, Stefano
Priolo, Manuela
Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome
title Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome
title_full Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome
title_fullStr Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome
title_full_unstemmed Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome
title_short Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome
title_sort characterization of cognitive, language and adaptive profiles of children and adolescents with malan syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316998/
https://www.ncbi.nlm.nih.gov/pubmed/35887841
http://dx.doi.org/10.3390/jcm11144078
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