Neuropediatrics 2009; 40(3): 137-140
DOI: 10.1055/s-0029-1237724
Short Communication

© Georg Thieme Verlag KG Stuttgart · New York

Association of Syndromic Mental Retardation and Autism with 22q11.2 Duplication

A. Lo-Castro1 , C. Galasso1 , C. Cerminara1 , N. El-Malhany1 , S. Benedetti1 , A. M. Nardone2 , P. Curatolo1
  • 1Department of Neuroscience, Paediatric Neurology Unit, “Tor Vergata” University of Rome, Rome, Italy
  • 2Department of Medical Genetics, “Tor Vergata” University of Rome, Rome, Italy
Further Information

Publication History

received 02.06.2009

accepted 27.07.2009

Publication Date:
17 December 2009 (online)

Abstract

We describe a 5.3-year-old girl with autism, mental retardation, hypotonia, marked speech delay, and mild dysmorphic features with a 22q11.2 duplication. Her mother carries the same duplication and presents cleft palate, and normal intelligence. The clinical and behavioural phenotype of this relatively new syndrome is very heterogeneous, with high variability also in the familiar cases. Up till now, about 50 cases of 22q11.2 duplication have been reported, but only three of them are associated with autistic disorders. We propose that in addition to 22q13.3 deletion syndrome, also 22q11.2 duplication should be suspected in a patient with unspecified dysmorphisms, mental retardation, autism, hypotonia, and severe speech delay.

References

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Correspondence

A. Lo-CastroMD 

Department of Neuroscience

Pediatric Neurology Unit

“Tor Vergata” University of Rome

Viale Oxford, 81

00133 Rome

Italy

Phone: +34/06/2090 0249

Fax: +34/06/2090 0018

Email: a.locastro@libero.it

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