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DOI: 10.1055/s-0029-1237724
© Georg Thieme Verlag KG Stuttgart · New York
Association of Syndromic Mental Retardation and Autism with 22q11.2 Duplication
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.
Key words
autism - 22q11.2 duplication - chromosome 22 - DiGeorge/velocardiofacial syndrome - mental retardation
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