| Literature DB >> 30968316 |
Pehlivanidis Artemios1, Spyropoulou Areti2, Papanikolaou Katerina3, Fryssira Helen4, Tsoytsoy Eirini4, Papageorgiou Charalambos2.
Abstract
Myhre syndrome (MS) is a connective tissue disorder with multisystem involvement with or without intellectual disability. In most cases SMAD4 mutations are reported. To date, 55 individuals have been molecularly confirmed. Autism has been proposed among associate clinical features of MS but no standardized diagnosis was available in previous cases. We report a case of a 25-year-old man with a pathogenic heterozygous SMAD4 missense mutation affecting residue Arg496 (SMAD4:p.Arg496Cys). Clinical findings are consistent with MS, commorbid with affective disorder and High Functioning Autism Spectrum Disorder confirmed by a standardized assessment procedure. The thorough clinical assessment of cases with syndromes such as MS can extend our knowledge on both the phenotypic characteristics of the syndrome and the genetic basis of autism.Entities:
Keywords: Affective disorder; High functioning autism spectrum disorder; Myhre syndrome; SMAD4 mutation
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Year: 2019 PMID: 30968316 DOI: 10.1007/s10803-019-04015-y
Source DB: PubMed Journal: J Autism Dev Disord ISSN: 0162-3257