Defining language disorders in children and adolescents with Noonan Syndrome

Giuseppe Zampino, Stefano Vicari, Giulia Lazzaro, Cristina Caciolo, Deny Menghini, Francesca Cumbo, Maria C. Digilio, Rossella Capolino, Marco Tartaglia, Paolo Alfieri

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review

Abstract

BACKGROUND: Noonan Syndrome is a developmental disorder characterized by a distinctive phenotype including facial dysmorphism, webbed neck, short stature, heart defects, and variable cognitive deficits as major features. Over the years, neuropsychological and behavioral studies explored alteration of cognitive functioning and related domains, such as learning, memory, and attention. To our knowledge, however, data concerning the language profile in this disorder is scarce. The aim of the present study was to detect specific language functioning combining nonverbal intelligence quotient and language abilities and to pinpoint strengths and weaknesses in the language domains. METHODS: The language profile of 37 Italian participants with molecularly confirmed diagnosis of Noonan Syndrome was evaluated using specific tools to assess vocabulary and grammar comprehension and production, as well as phonological development. RESULTS: We observed that 78% of affected individuals exhibited language impairment. Within language domains, the strong area was lexical production and grammar production was the weak area. Almost half the participants manifested a similar trend of specific language impairment. Nonverbal intelligence quotient only correlated with grammar comprehension. CONCLUSION: Our study expands present knowledge about the language profile in NS, and provides data that could enable more effective patient management and appropriate intervention.
Lingua originaleEnglish
pagine (da-a)e1069-N/A
RivistaMOLECULAR GENETICS & GENOMIC MEDICINE
DOI
Stato di pubblicazionePubblicato - 2020

Keywords

  • IQ
  • Linguistic functioning
  • PTPN11
  • RASopathies
  • SLI

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