Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a Coronin-1A mutation and a chromosome 16p11.2 deletion

Defects causing severe combined immunodeficiency (SCID) have been reported in pathways mediating antigen receptor rearrangement, antigen receptor and cytokine signaling, and purine metabolism. Recognizing that the actin regulator Coronin-1A is essential for development of a normal peripheral T cell...

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Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 131(2009), 1 vom: 09. Apr., Seite 24-30
1. Verfasser: Shiow, Lawrence R (VerfasserIn)
Weitere Verfasser: Paris, Kenneth, Akana, Matthew C, Cyster, Jason G, Sorensen, Ricardo U, Puck, Jennifer M
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Case Reports Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Microfilament Proteins coronin proteins 145420-64-0 DNA 9007-49-2
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245 1 0 |a Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a Coronin-1A mutation and a chromosome 16p11.2 deletion 
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520 |a Defects causing severe combined immunodeficiency (SCID) have been reported in pathways mediating antigen receptor rearrangement, antigen receptor and cytokine signaling, and purine metabolism. Recognizing that the actin regulator Coronin-1A is essential for development of a normal peripheral T cell compartment in mouse models, we identified absence of Coronin-1A in a girl with T-B+NK+ SCID who suffered recurrent infections including severe post-vaccination varicella at age 13 months. Murine Coronin-1A is essential for the release of T cells from the thymus, consistent with the paradoxically detectable thymus in our patient. Molecular analysis revealed a 2 bp deletion in the paternal CORO1A coding sequence paired with a 600 kb de novo deletion encompassing CORO1A on the maternal allele. This genomic region at 16p11.2 is subject to recurrent copy number variations associated with autism spectrum disorders, including attention deficit and hyperactivity, present in our patient. This case highlights the first link between actin cytoskeleton regulation and SCID 
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650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Research Support, Non-U.S. Gov't 
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700 1 |a Paris, Kenneth  |e verfasserin  |4 aut 
700 1 |a Akana, Matthew C  |e verfasserin  |4 aut 
700 1 |a Cyster, Jason G  |e verfasserin  |4 aut 
700 1 |a Sorensen, Ricardo U  |e verfasserin  |4 aut 
700 1 |a Puck, Jennifer M  |e verfasserin  |4 aut 
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