Phosphatase and Tensin Homolog (PTEN) Gene Mutations and Autism: Literature Review and a Case Report of a Patient With Cowden Syndrome, Autistic Disorder, and Epilepsy

Phosphatase and tensin homolog (PTEN) gene mutations are associated with a spectrum of clinical disorders characterized by skin lesions, macrocephaly, hamartomatous overgrowth of tissues, and an increased risk of cancers. Autism has rarely been described in association with these variable clinical f...

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Veröffentlicht in:Journal of Child Neurology 2012-03, Vol.27 (3), p.392-397
Hauptverfasser: Conti, Sara, Condò, Maria, Posar, Annio, Mari, Francesca, Resta, Nicoletta, Renieri, Alessandra, Neri, Iria, Patrizi, Annalisa, Parmeggiani, Antonia
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Sprache:eng
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