Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization. Issue 3 (24th December 2020)
- Record Type:
- Journal Article
- Title:
- Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization. Issue 3 (24th December 2020)
- Main Title:
- Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization
- Authors:
- Kopp, Nathan
Amarillo, Ina
Martinez‐Agosto, Julian
Quintero‐Rivera, Fabiola - Abstract:
- Abstract: Neuroligin 4 X‐linked ( NLGN4X ) is an X‐linked postsynaptic scaffolding protein, with functional role in excitatory synapsis development and maintenance, that has been associated with neuropsychiatric disorders such as intellectual disability, autism spectrum disorders (ASD), anxiety, attention deficit hyperactivity disorder (ADHD), and Tourette's syndrome. Chromosomal microarray analysis identified a paternally inherited, 445 Kb deletion on Xp22.3 that includes the entire NLGN4X in a 2.5 year old female (46, XX) with congenital hypotonia, strabismus, ASD, and increased aggressive behavioral issues. Her family history is significant for a mother with learning disabilities, a father with anxiety, major depressive disorder, and substance abuse, as well as two maternal half‐brothers with developmental delays. X‐inactivation studies in the proband's blood showed random X‐inactivation despite the presence of an abnormal X chromosome. Furthermore, trio exome sequencing did not reveal any other deleterious variant that could explain her phenotype. Our report describes the first example of a paternally inherited NLGN4X microdeletion as the genetic etiology of ASD in a female proband, and the psychiatric phenotypes in the father. It also provides further evidence that NLGN4X is sensitive to dosage changes in females, and can contribute to a variety of psychiatric features within the same family.
- Is Part Of:
- American journal of medical genetics. Volume 185:Issue 3(2021)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 185:Issue 3(2021)
- Issue Display:
- Volume 185, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 185
- Issue:
- 3
- Issue Sort Value:
- 2021-0185-0003-0000
- Page Start:
- 894
- Page End:
- 900
- Publication Date:
- 2020-12-24
- Subjects:
- autism -- clinical exome -- microarray -- microdeletion -- NLGN4X -- X inactivation
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.62025 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15802.xml