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Article

SDHD-related chromaffin tumours: disease localisation to genetic dysfunction.

Hormone research in paediatrics - 1 Jan 2010

Srirangalingam U, Khoo B, Matson M, Carpenter R, Reznek R, Maher E R, Chew S L, Drake W M

Abstract excerpt

BACKGROUND/AIMS: To describe the management of a subject with multiple chromaffin tumours found to have a novel succinate dehydrogenase D (SDHD) mutation. CASE: A 15-year-old boy with marked hypertension was found to have elevated urinary catecholamines and initial imaging thought to represent bilateral adrenal phaeochromocytomas. An adrenal venous catheter was required to clarify a right adrenal...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20190551
DOI: 10.1159/000277659

Genes

SDHD

Provenance

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