The First Vietnamese Patient of LEOPARD Syndrome due to a PTPN11 Mutation: A Case Report and Review of the Literature

LEOPARD syndrome is a rare congenital anomaly that involves several organs. Patients with this syndrome develop multiple lentigines resembling a leopard's hide. LEOPARD is an acronym of the major features constituting the syndrome including lentigines, electrocardiographic conduction defects, o...

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Detalles Bibliográficos
Autores principales: Nguyen, Hao Trong, Pham, Nguyen Nhat, Anh Vu, Hoang, Tran, Tu Nguyen Anh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452451/
https://www.ncbi.nlm.nih.gov/pubmed/34552798
http://dx.doi.org/10.1155/2021/8197435

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452451/
https://www.ncbi.nlm.nih.gov/pubmed/34552798
http://dx.doi.org/10.1155/2021/8197435

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