A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large Family
Gespeichert in:
Verfasser / Beitragende:
[A. Sexton, L. Rawlings, G. McKavanagh, K. Simons, I. Winship]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Genetic Counseling, 24/6(2015-12-01), 882-889
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.1007/s10897-015-9875-z |2 doi |
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| 245 | 0 | 2 | |a A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large Family |h [Elektronische Daten] |c [A. Sexton, L. Rawlings, G. McKavanagh, K. Simons, I. Winship] |
| 520 | 3 | |a We present a case where a variant of uncertain significance in the von Hippel Lindau syndrome gene (VHL) was identified in a proband with haemangioblastoma, and in a second degree relative with phaeochromocytoma. Initial uncertainty due to the unclear nature of the variant created psychosocial challenges for this family, in which four other genetic conditions were also present. Subsequent RNA studies confirmed this as a novel pathogenic mutation affecting splicing of exon 2. A third relative has since been diagnosed with haemangioblastoma. We suggest that this mutation possibly has reduced penetrance as there was no history of haemangioblastoma, renal tumours (apart from small cysts) or other VHL tumours among five mutation positive and seven untested adult relatives at 50% risk of the VHL mutation (average age 46years, range 18-70years). This case presents a novel VHL splicing mutation and highlights the psychosocial and medical value of additional laboratory studies on uncertain variants for individuals, their families and for the health professionals providing advice and counseling. | |
| 540 | |a National Society of Genetic Counselors, Inc., 2015 | ||
| 690 | 7 | |a Genetic counseling |2 nationallicence | |
| 690 | 7 | |a von Hippel Lindau syndrome |2 nationallicence | |
| 690 | 7 | |a Splicing mutation |2 nationallicence | |
| 690 | 7 | |a VUS |2 nationallicence | |
| 690 | 7 | |a Uncertainty |2 nationallicence | |
| 700 | 1 | |a Sexton |D A. |u Familial Cancer Centre, Royal Melbourne Hospital, 2-Centre, Grattan St, 3050, Parkville, VIC, Australia |4 aut | |
| 700 | 1 | |a Rawlings |D L. |u SA Pathology, Genetics & Molecular Pathology, Frome Rd, 5000, Adelaide, SA, Australia |4 aut | |
| 700 | 1 | |a McKavanagh |D G. |u SA Pathology, Genetics & Molecular Pathology, Frome Rd, 5000, Adelaide, SA, Australia |4 aut | |
| 700 | 1 | |a Simons |D K. |u SA Pathology, Genetics & Molecular Pathology, Frome Rd, 5000, Adelaide, SA, Australia |4 aut | |
| 700 | 1 | |a Winship |D I. |u Familial Cancer Centre, Royal Melbourne Hospital, 2-Centre, Grattan St, 3050, Parkville, VIC, Australia |4 aut | |
| 773 | 0 | |t Journal of Genetic Counseling |d Springer US; http://www.springer-ny.com |g 24/6(2015-12-01), 882-889 |x 1059-7700 |q 24:6<882 |1 2015 |2 24 |o 10897 | |
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| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Sexton |D A. |u Familial Cancer Centre, Royal Melbourne Hospital, 2-Centre, Grattan St, 3050, Parkville, VIC, Australia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Rawlings |D L. |u SA Pathology, Genetics & Molecular Pathology, Frome Rd, 5000, Adelaide, SA, Australia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a McKavanagh |D G. |u SA Pathology, Genetics & Molecular Pathology, Frome Rd, 5000, Adelaide, SA, Australia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Simons |D K. |u SA Pathology, Genetics & Molecular Pathology, Frome Rd, 5000, Adelaide, SA, Australia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Winship |D I. |u Familial Cancer Centre, Royal Melbourne Hospital, 2-Centre, Grattan St, 3050, Parkville, VIC, Australia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Journal of Genetic Counseling |d Springer US; http://www.springer-ny.com |g 24/6(2015-12-01), 882-889 |x 1059-7700 |q 24:6<882 |1 2015 |2 24 |o 10897 | ||