Profiling Cognitive and Social Functioning in a Small Cohort with Malan Syndrome

<b>Background/Objectives</b>: Malan syndrome (MALNS) is an ultra-rare genetic disorder caused by aberrations in the <i>NFIX</i> gene, located at chromosome 19p13.2. Key features of MALNS include general overgrowth, a typical facial gestalt, muscle–skeletal abnormalities, spee...

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Bibliographic Details
Main Authors: Niccolò Butti, Cosimo Urgesi, Paolo Alfieri, Manuela Priolo, Rosario Montirosso
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Children
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Online Access:https://www.mdpi.com/2227-9067/12/2/147
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