Case Report: Long-Term Treatment and Follow-Up of Kleefstra Syndrome-2
BackgroundMutations in the KMT2C gene can cause Kleefstra syndrome-2 (KLEFS2).CaseIn this study, we analyzed the clinical, genetic testing, and 10-year follow-up data of a child with KLEFS2 treated at the Child Healthcare Department, Children's Hospital of Nanjing Medical University, Nanjing. T...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2022-05-01
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| Series: | Frontiers in Pediatrics |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2022.881838/full |