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Probable Genetic Association Between Lhermitte-Duclos Disease/Cowden Syndrome and Autism Spectrum Disorder: A Case Report and Literature Comprehension

2025-12-17

Abstract excerpt

<h4>Background: </h4> Lhermitte-Duclos disease (LDD), known as dysplastic cerebellar gangliocytoma, is a hamartomatous lesion that causes progressive mass effect in the posterior fossa. Cowden syndrome (CS) is a rare autosomal dominant disorder characterized by an increased risk of developing various systemic malignancies. Both conditions result from mutations in the PTEN gene, which disrupts normal cell growth an...

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Literature Corpus work
481346ab-19b2-5d52-8b48-e02b59564cfa
DOI
10.20944/preprints202512.1411.v1
Open publication

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