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Malaysian Journal of Medicine and Health Sciences ; : 85-88, 2015.
Article in English | WPRIM | ID: wpr-625337

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.


Subject(s)
Genetic Association Studies
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