A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?

Pheochromocytoma is very rare at a pediatric age, and when it is present, the probability of a causative genetic mutation is high. Due to high costs of genetic surveys and an increasing number of genes associated with pheochromocytoma, a sequential genetic analysis driven by clinical and biochemical...

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Detalles Bibliográficos
Autores principales: Dias Pereira, Bernardo, Nunes da Silva, Tiago, Bernardo, Ana Teresa, César, Rui, Vara Luiz, Henrique, Pacak, Karel, Mota-Vieira, Luísa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884154/
https://www.ncbi.nlm.nih.gov/pubmed/29755524
http://dx.doi.org/10.1155/2018/8470642

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884154/
https://www.ncbi.nlm.nih.gov/pubmed/29755524
http://dx.doi.org/10.1155/2018/8470642

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