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Neuropsychological Genotype-Phenotype in Patients with Williams Syndrome with Atypical Deletions: A Systematic Review.

Neuropsychology review - 1 Dec 2023

Serrano-Juárez Carlos Alberto, Prieto-Corona Belén, Rodríguez-Camacho Mario, Sandoval-Lira Lucero, Villalva-Sánchez Ángel Fernando, Yáñez-Téllez Ma Guillermina, López María Fernanda Rangel

Abstract excerpt

Williams syndrome (WS) is a neurodevelopmental disorder caused by a microdeletion in the q11.23 region of chromosome 7. Recent case series reports and clinical case studies have suggested that the cognitive, behavioral, emotional, and social profile in WS could depend on the genes involved in the deletion. The objective of this systematic review was to analyze and synthesize the variability of the cognitive and...

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PMID: 36520254
DOI: 10.1007/s11065-022-09571-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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