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, ocular...
Main Authors: | Hao Trong Nguyen, Nguyen Nhat Pham, Hoang Anh Vu, Tu Nguyen Anh Tran |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2021-01-01
|
Series: | Case Reports in Genetics |
Online Access: | http://dx.doi.org/10.1155/2021/8197435 |
Similar Items
-
Melanoma and LEOPARD Syndrome: Understanding the Role of PTPN11 Mutations in Melanomagenesis
by: Rodolfo David Palacios-Diaz, et al.
Published: (2024-01-01) -
LEOPARD syndrome in an infant with severe hypertrophic cardiomyopathy and PTPN11 mutation
by: Ganigara Madhusudan, et al.
Published: (2011-01-01) -
PTPN11 Mutations in LEOPARD Syndrome: Report of Four Cases in Taiwan
by: I-Shou Lin, et al.
Published: (2009-10-01) -
LEOPARD Syndrome with a Sporadic PTPN11 Mutation in a Saudi Patient
by: Hussein M. Alshamrani, et al.
Published: (2023-01-01) -
LEOPARD syndrome with PTPN11 gene mutation in monozygotic twins: A case description and literature review
by: Yingwen Zhou, et al.
Published: (2025-02-01)