A Novel PTEN Frameshift Variant in a Child With Autism Spectrum Disorder and Macrocephaly: A Case Report

Margarida Moreno Fernandes1, Mariana Rodrigues Neto1, Mariana Sá Pinto1

  • 1Pediatrics, Unidade Local de Saúde Gaia/Espinho, Vila Nova de Gaia, PRT.

Cureus
|February 6, 2026
PubMed
Summary

PTEN hamartoma tumor syndrome (PHTS) is a rare genetic disorder. Early recognition in children with autism and macrocephaly is crucial for timely diagnosis and surveillance.

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