Document Detail


Mutation screening in a Norwegian cohort with pheochromocytoma.
MedLine Citation:
PMID:  23407919     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Pheochromocytomas (PHEOs) are neuroendocrine tumours, originating from chromaffin cells in the adrenal medulla. They are either sporadic or hereditary. It is important to identify the hereditary cases, so that patients and relatives with germline mutations can be offered regular surveillance. The objective of this study was the detection of pathogenic germline mutations in a cohort of Norwegian PHEO patients. Blood samples and/or formalin-fixed, paraffin-embedded tissue specimens, were collected from 60 patients who were operated upon between 1986 and 2004 at two university hospitals in Norway. DNA mutation analyses were performed successfully in the 42 blood samples and in one of the paraffin-embedded tissue specimen in VHL, RET, SDHB, SDHC, SDHD and NF1. In all, 32 different DNA variants were observed, of which 8 were classified as pathogenic (19 %), or possibly pathogenic; three in NF1, two in RET and VHL and one in SDHB. Two variants were observed in one patient, one in SDHB and one in NF1. Three of these variants are, to the best of our knowledge, new ones; two in NF1 [c.950_51insGCTGA, (p.Glu318LeufsX59) and c.1588G > A, (p.Val530Ile)] and one in VHL (c.308C > T, p.Pro103Leu). In conclusion the overall incidence of germline mutations in genes associated with familial PHEO was found to be of the same order of magnitude in the present Norwegian series as in those from other countries. Two new NF1 variants and one new VHL gene variant were detected.
Authors:
Wenche Sjursen; Henrik Halvorsen; Eva Hofsli; Siri Bachke; Asa Berge; Lars F Engebretsen; Sture E Falkmer; Ursula G Falkmer; Jan E Varhaug
Related Documents :
23528209 - The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous ...
23392799 - Lack of association between genetic polymorphisms in cytokine genes and tumor recurrenc...
24693539 - Tet2 overexpression in chronic lymphocytic leukemia is unrelated to the presence of tet...
24764719 - Lack of toxicity in a patient with germline tp53 mutation treated with radiotherapy.
23971939 - Irf5, but not tlr4, defeb1, or vdr, is associated with the risk of ulcerative colitis i...
23625609 - Genotypic and phenotypic features of japanese patients with mild to moderate hemophilia a.
21564629 - Tetranucleotide microsatellite loci from the black bear (ursus americanus).
11112379 - Phenotype determination of a common pro-leu polymorphism in human glutathione peroxidas...
20046399 - Genetic polymorphisms in dopamine- and serotonin-related genes and treatment responses ...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-2-14
Journal Detail:
Title:  Familial cancer     Volume:  -     ISSN:  1573-7292     ISO Abbreviation:  Fam. Cancer     Publication Date:  2013 Feb 
Date Detail:
Created Date:  2013-2-14     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100898211     Medline TA:  Fam Cancer     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Departments of Pathology and Medical Genetics, St Olav University Hospital, NO-7006, Trondheim, Norway, wenche.sjursen@stolav.no.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Low serum copeptin levels in patients with obstructive sleep apnea.
Next Document:  4D Ultrasound - Medical Devices for Recent Advances on the Etiology of Cerebral Palsy.