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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.


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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

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