Focusing on Autism Spectrum Disorder in Xia-Gibbs Syndrome: Description of a Female with High Functioning Autism and Literature Review.
Xia–Gibbs syndrome
autism spectrum disorder
genetic autism
Journal
Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936
Informations de publication
Date de publication:
26 May 2021
26 May 2021
Historique:
received:
26
04
2021
revised:
17
05
2021
accepted:
20
05
2021
entrez:
2
6
2021
pubmed:
3
6
2021
medline:
3
6
2021
Statut:
epublish
Résumé
Xia-Gibbs syndrome (XGS) is a rare disorder caused by de novo mutations in the AT-Hook DNA binding motif Containing 1 ( Here, we report on a girl patient who shows a peculiar cognitive and behavioural profile including high-functioning autism spectrum disorder (ASD) without intellectual disability and provide information on her developmental trajectory with the aim of expanding knowledge of the XGS clinical spectrum. On the basis of the current clinical case and the literature review, we also attempt to deepen understanding of behavioural and psychiatric manifestations associated with XGS. In addition to the patient we described, a considerable rate of individuals with XGS display autistic symptoms or have been diagnosed with an autistic spectrum disorder. Moreover, the analysis of the few psychopathological profiles of patients with XGS described in the literature shows a frequent presence of aggressive and self-injurious behaviours that could be either an expression of autistic functioning or an additional symptom of the ASD evolution. A careful investigation of the abovementioned symptoms is therefore required, since they could represent a "red flag" for ASD.
Sections du résumé
BACKGROUND
BACKGROUND
Xia-Gibbs syndrome (XGS) is a rare disorder caused by de novo mutations in the AT-Hook DNA binding motif Containing 1 (
METHODS
METHODS
Here, we report on a girl patient who shows a peculiar cognitive and behavioural profile including high-functioning autism spectrum disorder (ASD) without intellectual disability and provide information on her developmental trajectory with the aim of expanding knowledge of the XGS clinical spectrum. On the basis of the current clinical case and the literature review, we also attempt to deepen understanding of behavioural and psychiatric manifestations associated with XGS.
RESULTS
RESULTS
In addition to the patient we described, a considerable rate of individuals with XGS display autistic symptoms or have been diagnosed with an autistic spectrum disorder. Moreover, the analysis of the few psychopathological profiles of patients with XGS described in the literature shows a frequent presence of aggressive and self-injurious behaviours that could be either an expression of autistic functioning or an additional symptom of the ASD evolution. A careful investigation of the abovementioned symptoms is therefore required, since they could represent a "red flag" for ASD.
Identifiants
pubmed: 34073322
pii: children8060450
doi: 10.3390/children8060450
pmc: PMC8227570
pii:
doi:
Types de publication
Case Reports
Langues
eng
Références
Epilepsy Behav. 2021 Apr;117:107813
pubmed: 33642176
Cold Spring Harb Mol Case Stud. 2015 Oct;1(1):a000562
pubmed: 27148574
Dev Psychopathol. 2020 Oct;32(4):1287-1302
pubmed: 32677592
J Am Acad Child Adolesc Psychiatry. 2017 Jun;56(6):466-474
pubmed: 28545751
Cureus. 2020 Aug 9;12(8):e9622
pubmed: 32923223
J Autism Dev Disord. 2000 Jun;30(3):237-43
pubmed: 11055459
J Autism Dev Disord. 2011 Jul;41(7):926-37
pubmed: 20960041
Ann Lab Med. 2017 Nov;37(6):563-565
pubmed: 28841002
PLoS Med. 2009 Jul 21;6(7):e1000100
pubmed: 19621070
Am J Med Genet A. 2018 Jun;176(6):1315-1326
pubmed: 29696776
Am J Med Genet A. 2018 Sep;176(9):1890-1896
pubmed: 30152016
Yonsei Med J. 2014 Nov;55(6):1721-8
pubmed: 25323912
Epidemiol Psychiatr Sci. 2013 Sep;22(3):217-21
pubmed: 23531487
J Autism Dev Disord. 2019 Mar;49(3):845-856
pubmed: 30361939
ScientificWorldJournal. 2013 May 20;2013:158263
pubmed: 23766675
Am J Hum Genet. 2014 Mar 6;94(3):415-25
pubmed: 24581740
Cold Spring Harb Mol Case Stud. 2019 Jun 3;5(3):
pubmed: 30622101
Pediatr Rehabil. 2006 Jul-Sep;9(3):229-46
pubmed: 17050401
J Autism Dev Disord. 2010 Oct;40(10):1227-40
pubmed: 20195737
J Autism Dev Disord. 2012 Sep;42(9):1939-48
pubmed: 22310906
J Autism Dev Disord. 2010 Aug;40(8):1006-16
pubmed: 20143146
Eur J Med Genet. 2020 Jan;63(1):103637
pubmed: 30858058
Cureus. 2020 Dec 29;12(12):e12352
pubmed: 33520547
Int J Lang Commun Disord. 2010 Nov-Dec;45(6):681-90
pubmed: 20102259
J Speech Lang Hear Res. 2009 Jun;52(3):643-52
pubmed: 19380608
Dev Med Child Neurol. 2020 Jan;62(1):11
pubmed: 31621899
Am J Hum Genet. 2014 May 1;94(5):784-9
pubmed: 24791903
Mol Genet Genomic Med. 2019 Apr;7(4):e00596
pubmed: 30729726
Am J Med Genet A. 2021 Mar;185(3):990-994
pubmed: 33372375
Eur J Obstet Gynecol Reprod Biol. 2020 Jan;244:208-210
pubmed: 31812316
Mol Psychiatry. 2018 Feb;23(2):257-262
pubmed: 28242872
Nature. 2020 May;581(7806):19-21
pubmed: 32372044
J Autism Dev Disord. 2016 Jan;46(1):64-73
pubmed: 26231205
Res Dev Disabil. 2018 Dec;83:260-269
pubmed: 30368089
Iran J Med Sci. 2019 May;44(3):257-261
pubmed: 31182893
Eur J Med Genet. 2020 Jan;63(1):103611
pubmed: 30615951
J Child Neurol. 2015 Dec;30(14):1963-71
pubmed: 26374786
Hum Mutat. 2021 May;42(5):577-591
pubmed: 33644933
Eur J Neurosci. 2018 Mar;47(6):568-578
pubmed: 28112456
Mol Syndromol. 2017 Nov;8(6):308-312
pubmed: 29230160
J Autism Dev Disord. 2015 Jul;45(7):1978-88
pubmed: 25614020
Eur J Hum Genet. 2017 Dec;25(12):1364-1376
pubmed: 29158550
Mol Syndromol. 2020 Feb;11(1):24-29
pubmed: 32256298
Eur J Hum Genet. 2016 May;24(5):660-5
pubmed: 26350515