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...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Faculty of Medicine and Health Sciences, Universiti Putra Malaysia
2015
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| Online Access: | http://psasir.upm.edu.my/id/eprint/41700/ http://psasir.upm.edu.my/id/eprint/41700/1/A%20case%20of%20familial%20phaechromocytoma.pdf |
| _version_ | 1848849766332497920 |
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| author | Zahari Sham, Siti Yazmin Umar, Nor Aini Mazlan, Khalidah |
| author_facet | Zahari Sham, Siti Yazmin Umar, Nor Aini Mazlan, Khalidah |
| author_sort | Zahari Sham, Siti Yazmin |
| building | UPM Institutional Repository |
| collection | Online Access |
| 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. |
| first_indexed | 2025-11-15T09:55:36Z |
| format | Article |
| id | upm-41700 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T09:55:36Z |
| publishDate | 2015 |
| publisher | Faculty of Medicine and Health Sciences, Universiti Putra Malaysia |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-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 |
| spellingShingle | Zahari Sham, Siti Yazmin Umar, Nor Aini Mazlan, Khalidah A case of familial phaechromocytoma- was it? |
| title | 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_short | A case of familial phaechromocytoma- was it? |
| title_sort | case of familial phaechromocytoma- was it? |
| url | http://psasir.upm.edu.my/id/eprint/41700/ http://psasir.upm.edu.my/id/eprint/41700/1/A%20case%20of%20familial%20phaechromocytoma.pdf |