TY - JOUR
T1 - Developmental trends of communicative skills in children with chromosome 14 aberrations
AU - Zampini, L.
AU - Zanchi, Paola
AU - Rinaldi, B.
AU - Novara, F.
AU - Zuffardi, O.
PY - 2017
Y1 - 2017
N2 - Children with chromosome 14 aberrations usually show developmental delays, intellectual disability, neurological disorders and behaviour problems. The aim of the present study is to describe the developmental trajectories of the communicative skills of children with chromosome 14 aberrations, considering the possible relationships between the patterns of language development and the children’s clinical characteristics (e.g., intellectual disability or autistic traits). Longitudinal data on five children (four with linear deletions and one with ring 14 syndrome) followed for 3 years are presented. Four out of five children showed profound intellectual disability, and three out of five showed autistic traits. A high individual variability was found in both vocal and gestural productions. However, only a modest increase in the children’s communicative and symbolic skills was detected over time (e.g., in the quality of preverbal productions). Conclusion: The increase of communicative skills in children with chromosome 14 aberration is very slow. We need to consider the children’s characteristics, in terms of type of chromosome aberration, level of intellectual disability and presence/absence of autistic traits, to predict their possible linguistic outcomes and to give a more realistic expectation to their parents.What is known:• The communicative skills of children with chromosome 14 aberrations are usually impaired.• The presence of autistic traits is frequent in these children.What is new:• The increase of communicative skills in children with chromosome 14 aberrations is very slow.• The level of intellectual disability and the presence/absence of autistic traits appeared to have a role in predicting the possible linguistic outcomes in children with chromosome 14 aberrations.
AB - Children with chromosome 14 aberrations usually show developmental delays, intellectual disability, neurological disorders and behaviour problems. The aim of the present study is to describe the developmental trajectories of the communicative skills of children with chromosome 14 aberrations, considering the possible relationships between the patterns of language development and the children’s clinical characteristics (e.g., intellectual disability or autistic traits). Longitudinal data on five children (four with linear deletions and one with ring 14 syndrome) followed for 3 years are presented. Four out of five children showed profound intellectual disability, and three out of five showed autistic traits. A high individual variability was found in both vocal and gestural productions. However, only a modest increase in the children’s communicative and symbolic skills was detected over time (e.g., in the quality of preverbal productions). Conclusion: The increase of communicative skills in children with chromosome 14 aberration is very slow. We need to consider the children’s characteristics, in terms of type of chromosome aberration, level of intellectual disability and presence/absence of autistic traits, to predict their possible linguistic outcomes and to give a more realistic expectation to their parents.What is known:• The communicative skills of children with chromosome 14 aberrations are usually impaired.• The presence of autistic traits is frequent in these children.What is new:• The increase of communicative skills in children with chromosome 14 aberrations is very slow.• The level of intellectual disability and the presence/absence of autistic traits appeared to have a role in predicting the possible linguistic outcomes in children with chromosome 14 aberrations.
KW - Autistic traits
KW - Chromosome 14 aberrations
KW - Communication
KW - Intellectual disability
KW - Longitudinal
KW - Ring 14 syndrome
KW - Autistic traits
KW - Chromosome 14 aberrations
KW - Communication
KW - Intellectual disability
KW - Longitudinal
KW - Ring 14 syndrome
UR - https://publicatt.unicatt.it/handle/10807/251775
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85010777925&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85010777925&origin=inward
U2 - 10.1007/s00431-017-2859-2
DO - 10.1007/s00431-017-2859-2
M3 - Article
SN - 0340-6199
VL - 176
SP - 455
EP - 464
JO - European Journal of Pediatrics
JF - European Journal of Pediatrics
IS - 4
ER -