Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review
- PMID: 20830797
- DOI: 10.1002/ajmg.a.33573
Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review
Abstract
The screening of individuals with mild dysmorphic features and mental retardation using whole genome scanning technologies has resulted in the delineation of several previously unrecognized microdeletion syndromes. Microdeletion of 3q29 has been recently described as one such new syndrome. The clinical phenotype is variable despite an almost identical submicroscopic deletion size in most cases. We report on two individuals that further expand the clinical presentation of this rare disorder and compare the findings with earlier reports to refine the 3q29 microdeletion syndrome phenotype. The propositi are a 10-year-old female and a 15-year-old male, who have in common intellectual disabilities, a history of autism and psychiatric symptoms ranging from bipolar disorder presenting with increasing suicidal ideation to aggressive behavior and general anxiety. Other shared physical findings include asymmetric face, high-nasal bridge, crowded/dysplastic teeth, and tapered fingers. Oligonucleotide array-based chromosomal microarray analysis (CMA) using a genome-wide SNP array identified a de novo subtelomeric microdeletion of chromosome region 3q29 ranging from 1.6 to 2.1 Mb. The region of overlap encompasses 20 RefSeq genes, including FBX045, DLG1, and PAK2. These genes are related to neuronal postsynaptic membrane function and PTEN signaling, suggesting a role for synaptic connectivity dysfunction in the etiology of autism in these children. The novel clinical presentation of our patients expands the clinical spectrum of the 3q29 microdeletion syndrome and provides additional insights into the pathophysiology of autism and psychiatric disorders.
Copyright © 2010 Wiley-Liss, Inc.
Similar articles
-
Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.Am J Med Genet A. 2013 Apr;161A(4):845-9. doi: 10.1002/ajmg.a.35754. Epub 2013 Feb 26. Am J Med Genet A. 2013. PMID: 23443968 Free PMC article.
-
3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.Am J Med Genet A. 2013 Dec;161A(12):3018-22. doi: 10.1002/ajmg.a.36142. Epub 2013 Sep 24. Am J Med Genet A. 2013. PMID: 24214349
-
[Identification of a novel deletion region in 3q29 microdeletion syndrome by oligonucleotide array comparative genomic hybridization].Korean J Lab Med. 2010 Feb;30(1):70-5. doi: 10.3343/kjlm.2010.30.1.70. Korean J Lab Med. 2010. PMID: 20197726 Korean.
-
A clinical case report and literature review of the 3q29 microdeletion syndrome.Clin Dysmorphol. 2015 Jul;24(3):89-94. doi: 10.1097/MCD.0000000000000077. Clin Dysmorphol. 2015. PMID: 25714563 Free PMC article. Review.
-
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.Genet Med. 2007 Sep;9(9):607-16. doi: 10.1097/gim.0b013e3181484b49. Genet Med. 2007. PMID: 17873649 Review.
Cited by
-
Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.Am J Med Genet A. 2013 Apr;161A(4):845-9. doi: 10.1002/ajmg.a.35754. Epub 2013 Feb 26. Am J Med Genet A. 2013. PMID: 23443968 Free PMC article.
-
Behavioral Phenotypes and Comorbidity in 3q29 Deletion Syndrome: Results from the 3q29 Registry.J Autism Dev Disord. 2025 Feb;55(2):667-677. doi: 10.1007/s10803-023-06218-w. Epub 2024 Jan 12. J Autism Dev Disord. 2025. PMID: 38216835 Free PMC article.
-
Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era.Appl Clin Genet. 2012 Feb 20;5:1-18. doi: 10.2147/TACG.S21953. Appl Clin Genet. 2012. PMID: 23144566 Free PMC article.
-
A Genome-Wide Association Study and Complex Network Identify Four Core Hub Genes in Bipolar Disorder.Int J Mol Sci. 2017 Dec 19;18(12):2763. doi: 10.3390/ijms18122763. Int J Mol Sci. 2017. PMID: 29257106 Free PMC article.
-
Neural Mechanisms Underlying Repetitive Behaviors in Rodent Models of Autism Spectrum Disorders.Front Cell Neurosci. 2021 Jan 14;14:592710. doi: 10.3389/fncel.2020.592710. eCollection 2020. Front Cell Neurosci. 2021. PMID: 33519379 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous