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Region 17p13 Allelic Loss Associated Medulloblastoma

MedGen UID:
233916
•Concept ID:
C1335732
•
Neoplastic Process

Definition

A medulloblastoma characterized by the loss of one of the p13 regions of chromosome 17. Loss of genetic material of chromosome arm 17p is the most common molecular genetic abnormality found in medulloblastomas. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVRegion 17p13 Allelic Loss Associated Medulloblastoma

Recent clinical studies

Clinical prediction guides

Molecular genetic studies in medulloblastomas: evidence for tumor suppressor genes at the chromosomal regions 1q31-32 and 17p13.
Pietsch T, Koch A, Wiestler OD
Klin Padiatr 1997 Jul-Aug;209(4):150-5. doi: 10.1055/s-2008-1043965. PMID: 9293446
Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors.
Biegel JA, Burk CD, Barr FG, Emanuel BS
Cancer Res 1992 Jun 15;52(12):3391-5. PMID: 1596898

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