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Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma

Overview of attention for article published in Current Opinion in Endocrinology Diabetes and Obesity, June 2014
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Title
Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma
Published in
Current Opinion in Endocrinology Diabetes and Obesity, June 2014
DOI 10.1097/med.0000000000000059
Pubmed ID
Authors

Huma Q. Rana, Irene R. Rainville, Anand Vaidya

Abstract

Paraganglioma and pheochromocytoma (PGL/PCC) are tumours of neural crest origin that can present along a clinical spectrum ranging from apparently sporadic, isolated tumours to a more complex phenotype of one or multiple tumours in the context of other clinical features and family history suggestive of a defined hereditary syndrome. Genetic testing for hereditary PGL/PCC can help to confirm a genetic diagnosis for sporadic and syndromic cases. Informative genetic testing serves to clarify future risks for the patient and family members.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 22 100%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 5 23%
Researcher 5 23%
Student > Master 3 14%
Student > Ph. D. Student 3 14%
Student > Doctoral Student 1 5%
Other 3 14%
Unknown 2 9%
Readers by discipline Count As %
Medicine and Dentistry 13 59%
Agricultural and Biological Sciences 3 14%
Nursing and Health Professions 1 5%
Social Sciences 1 5%
Biochemistry, Genetics and Molecular Biology 1 5%
Other 0 0%
Unknown 3 14%