A case of familial phaechromocytoma- was it?

Citation

Zahari Sham, Siti Yazmin and Umar, Nor Aini and Mazlan, Khalidah (2015) A case of familial phaechromocytoma- was it? Malaysian Journal of Medicine and Health Sciences, 11 (2). art. no. http://www.medic.upm.edu.my/dokumen/FKUSK1_Final_Article_9.pdf. pp. 85-88. ISSN 1675-8544

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.

Download File

Preview

PDF
A case of familial phaechromocytoma.pdf
Download (650kB) | Preview

Additional Metadata

Item Type:	Article
Divisions:	Faculty of Medicine and Health Science
Publisher:	Faculty of Medicine and Health Sciences, Universiti Putra Malaysia
Keywords:	Familial; Phaechromocytoma; Phenotype-genotype correlations
Depositing User:	Mohd Hafiz Che Mahasan
Date Deposited:	01 Feb 2016 07:18
Last Modified:	01 Feb 2016 07:18
URI:	http://psasir.upm.edu.my/id/eprint/41700
Statistic Details:	View Download Statistic

Actions (login required)

View Item