Format

Send to:

Choose Destination
See comment in PubMed Commons below
Eur J Med Genet. 2012 Jan;55(1):32-6. doi: 10.1016/j.ejmg.2011.08.004. Epub 2011 Sep 10.

IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.

Author information

  • 1Department of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, KS, United States. eyoungs@saint-lukes.org

Abstract

Intellectual disability affects approximately 2% of the population with males outnumbering females due to involvement of over 300 genes on the X chromosome. The most common form of X-linked intellectual disability (XLID) is fragile X syndrome. We report a family with an apparent XLID pattern with the proband, his mother and maternal half brother having an Xp21.3 deletion detected with chromosomal microarray analysis involving the interleukin 1 receptor accessory protein-like 1 (IL1RAPL1) gene. IL1RAPL1 is highly expressed in the postnatal brain, specifically hippocampus suggesting a specialized role in memory and learning abilities. The proband presented with intellectual disability, a broad face, prominent and wide nasal root, ptosis, a wide philtrum and a small mouth. XLID due to involvement of the IL1RAPL1 gene has been reported to cause nonsyndromic XLID. We report a new family with XLID due to partial deletion of IL1RAPL1, summarize reported literature and describe similar phenotypic similarities among the affected individuals in this family and those reported in the literature proposing that deletion of IL1RAPL1 may cause syndromic XLID. Additional reports are needed to further characterize whether syndromic features are related to disturbances of this gene.

Copyright © 2011 Elsevier Masson SAS. All rights reserved.

PMID:
21933724
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Elsevier Science
    Loading ...
    Write to the Help Desk