TY - JOUR
T1 - Lenguaje de niños y jóvenes con síndrome de deleción 22q11
AU - Brun-Gasca, Carme
AU - Fornieles-Deu, Albert
AU - Sebastián-Lázaro, Diana
N1 - Publisher Copyright:
© 2020 Revista de Neurología
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Introduction. The 22q11 deletion syndrome (S22q11) is one of the most prevalent genetic disorders, resulting in multiple systemic and neuropsychological features. Aim. To describe the language profile in a sample of Spanish subjects with S22q11. Patients and methods. A sample of 30 Spanish participants with S22q11 aged between 5 years and 21 years and 11 months (mean: 12.14 ± 4.20 years) was evaluated using standardized tests and a questionnaire administered to parents. Results. Almost half of the subjects obtained better results in expressive language than in comprehensive language and the majority obtained a higher score in language content than in language memory. The results suggest that people with S22q11 present language difficulties that improve with age to a certain level and subsequently stabilize. A specific profile is observed that suggests that pragmatic difficulties are a consequence of this language profile and not only of social difficulties already described in this pathology. Conclusions. In the sample of the present study, children and young people with S22q11 present specific language and pragmatic disorders. More than half of the study participants did not obtain significant differences between the level of expressive and receptive language. Most presented semantic fluency difficulties. The type and degree of impairment in pragmatic skills suggest that the basic problem may be related to their language difficulties.
AB - Introduction. The 22q11 deletion syndrome (S22q11) is one of the most prevalent genetic disorders, resulting in multiple systemic and neuropsychological features. Aim. To describe the language profile in a sample of Spanish subjects with S22q11. Patients and methods. A sample of 30 Spanish participants with S22q11 aged between 5 years and 21 years and 11 months (mean: 12.14 ± 4.20 years) was evaluated using standardized tests and a questionnaire administered to parents. Results. Almost half of the subjects obtained better results in expressive language than in comprehensive language and the majority obtained a higher score in language content than in language memory. The results suggest that people with S22q11 present language difficulties that improve with age to a certain level and subsequently stabilize. A specific profile is observed that suggests that pragmatic difficulties are a consequence of this language profile and not only of social difficulties already described in this pathology. Conclusions. In the sample of the present study, children and young people with S22q11 present specific language and pragmatic disorders. More than half of the study participants did not obtain significant differences between the level of expressive and receptive language. Most presented semantic fluency difficulties. The type and degree of impairment in pragmatic skills suggest that the basic problem may be related to their language difficulties.
KW - 22q11 deletion syndrome. Language. Pragmatics. Rare disease. Speech therapy. Velocardiofacial syndrome
UR - http://www.scopus.com/inward/record.url?scp=85088158578&partnerID=8YFLogxK
UR - https://dialnet.unirioja.es/servlet/articulo?codigo=7532288
U2 - 10.33588/RN.7103.2020145
DO - 10.33588/RN.7103.2020145
M3 - Artículo
C2 - 32672348
AN - SCOPUS:85088158578
SN - 0210-0010
VL - 71
SP - 99
EP - 109
JO - Revista de Neurologia
JF - Revista de Neurologia
IS - 3
ER -