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Case Report: Long-Term Treatment and Follow-Up of Kleefstra Syndrome-2

BACKGROUND: Mutations in the KMT2C gene can cause Kleefstra syndrome-2 (KLEFS2). CASE: In 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, Nanji...

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Detalles Bibliográficos
Autores principales:	Wu, Dandan, Li, Rong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172761/ https://www.ncbi.nlm.nih.gov/pubmed/35685914 http://dx.doi.org/10.3389/fped.2022.881838

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