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...

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Egile Nagusiak: Dandan Wu (Egilea), Rong Li (Egilea)
Formatua: Liburua
Argitaratua: Frontiers Media S.A., 2022-05-01T00:00:00Z.
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