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A case of familial phaechromocytoma- was it?

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 h...

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Main Authors: Zahari Sham, Siti Yazmin, Umar, Nor Aini, Mazlan, Khalidah
Format: Article
Language:English
Published: Faculty of Medicine and Health Sciences, Universiti Putra Malaysia 2015
Online Access:http://psasir.upm.edu.my/id/eprint/41700/1/A%20case%20of%20familial%20phaechromocytoma.pdf
http://psasir.upm.edu.my/id/eprint/41700/
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spelling my.upm.eprints.417002016-02-01T07:18:15Z http://psasir.upm.edu.my/id/eprint/41700/ A case of familial phaechromocytoma- was it? Zahari Sham, Siti Yazmin Umar, Nor Aini Mazlan, Khalidah 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. Faculty of Medicine and Health Sciences, Universiti Putra Malaysia 2015-06 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/41700/1/A%20case%20of%20familial%20phaechromocytoma.pdf 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
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description 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.
format Article
author Zahari Sham, Siti Yazmin
Umar, Nor Aini
Mazlan, Khalidah
spellingShingle Zahari Sham, Siti Yazmin
Umar, Nor Aini
Mazlan, Khalidah
A case of familial phaechromocytoma- was it?
author_facet Zahari Sham, Siti Yazmin
Umar, Nor Aini
Mazlan, Khalidah
author_sort Zahari Sham, Siti Yazmin
title A case of familial phaechromocytoma- was it?
title_short A case of familial phaechromocytoma- was it?
title_full A case of familial phaechromocytoma- was it?
title_fullStr A case of familial phaechromocytoma- was it?
title_full_unstemmed A case of familial phaechromocytoma- was it?
title_sort case of familial phaechromocytoma- was it?
publisher Faculty of Medicine and Health Sciences, Universiti Putra Malaysia
publishDate 2015
url http://psasir.upm.edu.my/id/eprint/41700/1/A%20case%20of%20familial%20phaechromocytoma.pdf
http://psasir.upm.edu.my/id/eprint/41700/
_version_ 1643833073669767168
score 13.223943

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