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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.
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.
Area of Science:
- Genetics
- Pediatrics
- Neurology
Background:
- PTEN hamartoma tumor syndrome (PHTS) is a rare genetic condition linked to neurodevelopmental disorders, macrocephaly, and cancer predisposition.
- Children with PHTS often present with a range of symptoms, including developmental delays and macrocephaly.
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