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Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC
Stephan Niemann1, Ulrich Müller, Dieter Engelhardt
1Institut für Humangenetik, Justus-Liebig-Universität, Schlangenzahl 14, 35392, Giessen, Germany. Stephan.Niemann@humangenetik.med.uni-giessen.de
Abstract:
Mutations in SDHC cause autosomal dominant paraganglioma, type 3 (PGL3), and have to date been demonstrated in only one family. Here, we report on a novel mutation in a patient with a malignant, catecholamine-producing paraganglioma at the carotid bifurcation. The mutation is a G-->T transversion at position +1 of intron 5 of the SDHC gene, leading to the deletion of exon 5 and a shift in the reading frame.
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