No evidence for increased mortality in SDHD variant carriers compared with the general population-Reference-Cited by-同舟云学术

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No evidence for increased mortality in SDHD variant carriers compared with the general population

Published:2015-03-11 Issue:12 Volume:23 Page:1713-1716
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

van Hulsteijn Leonie T,Heesterman Berdine,Jansen Jeroen C,Bayley Jean-Pierre,Hes Frederik J,Corssmit Eleonora P M,Dekkers Olaf M

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg201536.pdf

Reference32 articles.

1. Baysal BE, Ferrell RE, Willett-Brozick JE et al: Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 2000; 287: 848–851.

2. Benn DE, Gimenez-Roqueplo AP, Reilly JR et al: Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. J Clin Endocrinol Metab 2006; 91: 827–836.

3. Hensen EF, Siemers MD, Jansen JC et al: Variants in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients. Clin Endocrinol (Oxf) 2011; 75: 650–655.

4. van Hulsteijn LT, den Dulk AC, Hes FJ, Bayley JP, Jansen JC, Corssmit EP : No difference in phenotype of the main Dutch SDHD founder variants. Clin Endocrinol (Oxf) 2013; 79: 824–831.

5. Jansen JC, van den Berg R, Kuiper A, van der Mey AG, Zwinderman AH, Cornelisse CJ : Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal. Cancer 2000; 88: 2811–2816.

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1. Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants;The Lancet Diabetes & Endocrinology;2023-05

2. Feasibility and safety of the posterior retroperitoneoscopic approach in the resection of aortocaval and infrarenal paraganglioma: a single-center experience;Surgical Endoscopy;2021-08-02

3. Increased Mortality in SDHB but Not in SDHD Pathogenic Variant Carriers;Cancers;2019-01-17

4. Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma;Journal of Internal Medicine;2018-12-08

5. Phéochromocytomes et paragangliomes génétiquement déterminés: quelle conduite à tenir chez les apparentés ?;Annales d'Endocrinologie;2018-09

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