Longitudinal imaging in Kleefstra syndrome—Brief report and literature review
Abstract Background Kleefstra syndrome (KS) is a rare genetic condition affecting the euchromatic histone methyltransferase 1 (EHMT1) gene, typically presenting with developmental delay, generalized hypotonia, distinctive facial dysmorphisms, and neuropsychiatric anomalies. Methods We collected long...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2023-09-01
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| Series: | Annals of the Child Neurology Society |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/cns3.20032 |
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