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Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism
Authors:Gulhan Ercan-Sencicek A  Davis Wright Nicole R  Frost Stephen J  Fulbright Robert K  Felsenfeld Susan  Hart Lesley  Landi Nicole  Einar Mencl W  Sanders Stephan J  Pugh Kenneth R  State Matthew W  Grigorenko Elena L
Affiliation:Program on Neurogenetics, Yale University School of Medicine, USA.
Abstract:
Potocki-Lupski syndrome (PTLS; OMIM 610883) is a genomic syndrome that arises as a result of a duplication of 17p11.2. Although numerous cases of individuals with PTLS have been presented in the literature, its behavioral characterization is still ambiguous. We present a male child with a de novo dup(17)(p11.2p11.2) and he does not possess any autistic features, but is characterized by severe speech and language impairment. In the context of the analyses of this patient and other cases of PTLS, we argue that the central feature of the syndrome appears to be related to diminished speech and language capacity, rather than the specific social deficits central to autism.
Keywords:Language and speech impairment   Potocki–Lupski syndrome   17p11.2, EFCBP1   inv(8)(q21.3-q24.1)
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