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• W2206949238 abstract "Simpson–Golabi–Behmel syndrome (SGBS) is an X‐linked condition characterized by pre and post natal overgrowth, facial malformations, and visceral, skeletal, and neurological anomalies. The physical characteristics of SGBS have been well documented; however there is a lack of description regarding the behavioral phenotype. We report the case of a 6‐year‐old boy, with confirmed deletion of 6–8 exons of the glypican‐3 gene ( GPC3 ) who presents three distinctive findings: the persistence of the craniopharyngeal canal, an immune‐allergic specificity, and a scarcely behavioral phenotype consisting in the association of Austim Spectrum Disorder with accompanying mild intellectual disability and language impairments. He also fulfilled the criteria of Attention Deficit Hyperactivity Disorder and Oppositional Defiant Disorder according to DSM 5 criteria. The specificities of the case are discussed in the light of recent pathophysiological data. © 2015 Wiley Periodicals, Inc." @default.
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• W2206949238 date "2015-12-22" @default.
• W2206949238 modified "2023-09-27" @default.
• W2206949238 title "Distinctive findings in a boy with Simpson-Golabi-Behmel syndrome" @default.
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• W2206949238 doi "https://doi.org/10.1002/ajmg.a.37518" @default.
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