Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in Singapore

BACKGROUND: Hereditary paraganglioma (PGL) and pheochromocytoma (PCC) syndromes are rare conditions, with limited data on spectrum of causative gene variants of these syndromes in Asian patients. METHODS: We describe the clinical characteristics and genetic testing outcomes of patients with suspecte...

Descripción completa

Detalles Bibliográficos
Autores principales: Ting, Kay Reen, Ong, Pei Yi, Wei, Samuel Ow Guan, Parameswaran, Rajeev, Khoo, Chin Meng, Deepak, Doddabele Srinivasa, Lee, Soo-Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731464/
https://www.ncbi.nlm.nih.gov/pubmed/33308260
http://dx.doi.org/10.1186/s13053-020-00156-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731464/
https://www.ncbi.nlm.nih.gov/pubmed/33308260
http://dx.doi.org/10.1186/s13053-020-00156-9

Ejemplares similares