Articles with "ppgl patients" as a keyword



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Genetic and Clinical Profiles of Pheochromocytoma and Paraganglioma: A Single Center Study

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Published in 2020 at "Frontiers in Endocrinology"

DOI: 10.3389/fendo.2020.574662

Abstract: Pheochromocytoma/paraganglioma (PPGL) has a high genetic heterogeneity with 40% germline variants in known pathogenic genes. Data in Chinese on this aspect are scanty. To detect the genetic and clinical profile of Chinese PPGL patients, we… read more here.

Keywords: chinese ppgl; genetic clinical; ppgl patients; ppgl ... See more keywords
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Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population.

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Published in 2020 at "Endocrinology and metabolism"

DOI: 10.3803/enm.2020.683

Abstract: BACKGROUND Pheochromocytoma and paragangliomas (PPGL) are hereditary in approximately 30% to 40% cases. With the advancement of genetic analysis techniques, including next-generation sequencing (NGS), there were attempts to classify PPGL into molecular clusters. With NGS… read more here.

Keywords: pheochromocytoma; ppgl patients; clinical characteristics; germline mutations ... See more keywords