A Case of Familial Phaechromocytoma- Was It?
Malaysian Journal of Medicine and Health Sciences
; : 85-88, 2015.
Article
Dans En
| WPRIM
| ID: wpr-625337
Responsable en Bibliothèque :
WPRO
ABSTRACT
With advancement in genetic studies, familial phaeochromocytoma (PCC) and paraganglioma (PGL) are increasingly being recognized. Characteristically, correlations exist between genotypes and clinical and biochemical phenotypes. We report a phaeochromocytoma in a young patient with intriguing family histories, raising the possibility of his being a familial case.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Études d'associations génétiques
Type d'étude:
Prognostic_studies
langue:
En
Texte intégral:
Malaysian Journal of Medicine and Health Sciences
Année:
2015
Type:
Article