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