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Brief Report: Evidence of Autism Spectrum Disorder Caused by a Mutation in ATRX Gene: A Case Report.
- 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.)
- Subjects :
- Humans
DNA Helicases genetics
X-linked Nuclear Protein genetics
Mutation
alpha-Thalassemia diagnosis
alpha-Thalassemia genetics
alpha-Thalassemia complications
Autism Spectrum Disorder diagnosis
Autism Spectrum Disorder genetics
Autism Spectrum Disorder complications
X-Linked Intellectual Disability diagnosis
X-Linked Intellectual Disability genetics
X-Linked Intellectual Disability complications
Intellectual Disability genetics
Intellectual Disability complications
Subjects
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