Collect whole blood in a purple top (EDTA) tube.
Refrigerate sample until shipment. Send the sample at room temperature with overnight delivery for receipt Monday through Friday within 24 hours of collection.
Whole blood can be refrigerated until shipment.
Heparinized specimens, severely hemolyzed specimens, frozen, clotted or possibly commingled specimens, blood in non-sterile or leaky containers, mislabeled or inappropriately labeled specimens.
Do not heat, freeze or centrifuge blood before shipment. Refrigerate sample until shipment.
Mon - Fri 9:00am to 4:00pm
Paraganglioma syndrome includes inherited head and neck paragangliomas
(HNPs) and adrenal or extra-adrenal pheochromocytomas. Hereditary paragangliomas belong to a group of dominantly inherited disorders characterized by the development of highly vascularized, nonchromaffin tumors arising in parasympathetic ganglia, usually in the head and neck. Up to 50% of paragangliomas are familial, and multiple loci are known to be involved. The genes responsible for familial paraganglioma / pheochromocytoma (PGL/PCC) syndromes encode three of the four subunits of the succinate-dehydrogenase (SDH) mitochondrial enzyme complex: SDHB, SDHC and SDHD.
Succinate-dehydrogenase is involved in oxidation of succinate to fumarate in the Krebs cycle and in providing electrons to the mitochondrial electron transport chain. SDHC and SDHD proteins anchor complex II in the inner mitochondrial membrane while SDHB encodes one of the two subunits of the catalytic core, the iron-sulphur protein.
SDHB (1p25) is composed of eight exons and is approximately 40 kb in length. Nonsense, missense, and splice-site mutations, intragenic deletions and insertions, and whole-gene SDHB deletions have been reported in individuals affected with hereditary paraganglioma syndromes.
SDHC (1q21) has six exons and is more than 35 kb in length. Nonsense, missense, splice-site, regulatory, and exon deletions have been reported in individuals affected with hereditary PGL syndromes.
SDHD (11q23) consists of four exons that encodes a 1313-bp transcript. Nonsense, missense, splice-site, intragenic insertions and deletions, and a whole-gene deletion have been reported in SDHD in individuals affected with hereditary paraganglioma syndromes.
Large deletions and duplications in the SDHB/SDHC/SDHD genes will be detected using multiplex ligation-dependent probe amplification assay (MLPA).
Although data regarding the frequency of exonic, multiexonic, or whole-gene deletions in SDHB, SDHC, and SDHD are limited, such deletions have been reported in all three genes. Deletions in the SDHB gene are identified in 12% of individuals in whom sequence results are negative. The analytical senstivity of MLPA is ~99%.
We offer DNA sequence analysis of the SDHB, SDHC and SDHD genes.
Known mutation analysis is available to family members for previously identified mutations.
Prenatal testing is available for individuals who are confirmed carriers of mutations. Please contact the laboratory director to discuss appropriate testing prior to collecting a prenatal specimen.
We offer the following tests related to Pheochromocytoma:
Multiple Endocrine Neoplasia type 2 - MEN2A and MEN2B analysis (exons 16 -19).
Von-Hippel-Lindau Disease – VHL Gene Sequencing and Deletion Analysis
Test results with interpretation will be mailed and/or faxed to the referring physician or send out lab following completion of the test. Additional reports will be provided as requested.
Molecular diagnosis of affected individuals allows pre-symptomatic screening of at risk family members and leads to early detection and timely intervention in the disease process.
Whole blood in EDTA purple top tubes is the preferred sample. High molecular weight genomic DNA, cheek epithelial cells, or other samples containing DNA may be acceptable. Contact the laboratory for specific instructions regarding such samples before sending the sample.