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Brief Report: Evidence of Autism Spectrum Disorder Caused by a Mutation in ATRX Gene: A Case Report.

Authors :
López-Garrido MP
Carrascosa-Romero MC
Montero-Hernández M
Ruiz-Almansa J
Sánchez-Sánchez F
Source :
Journal of autism and developmental disorders [J Autism Dev Disord] 2024 Jan; Vol. 54 (1), pp. 379-388. Date of Electronic Publication: 2022 May 20.
Publication Year :
2024

Abstract

ATRX mutations are commonly associated with alpha-thalassaemia mental retardation syndrome (ATR-X syndrome) with a notable variable expressivity. This X-linked disorder is characterized by intellectual disability (ID) in a higher or lesser degree, in which the alpha-thalassaemia feature is not always present. Other phenotypic manifestations like facial dimorphism, hypotonia, microcephaly, skeletal abnormalities or urogenital malformations have been frequently observed in ATR-X syndrome. Herein, we report a missense ATRX mutation (Thr1621Met) in a patient with an autism spectrum disorder (ASD) diagnosis. Except for ID, no typical signs of ATR-X syndrome were found in the patient. These results confirm the extensive phenotypic variability associated to ATRX mutations and show the involvement of this gene in the ASD.<br /> (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Details

Language :
English
ISSN :
1573-3432
Volume :
54
Issue :
1
Database :
MEDLINE
Journal :
Journal of autism and developmental disorders
Publication Type :
Academic Journal
Accession number :
35593993
Full Text :
https://doi.org/10.1007/s10803-022-05588-x