Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma.

2.50
Hdl Handle:
http://hdl.handle.net/10541/99959
Title:
Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma.
Authors:
Evans, D Gareth R; Burnell, Liza D; Campbell, R; Gattamaneni, Rao; Birch, Jillian M
Abstract:
One hundred seventy-three consecutive cases of medulloblastoma recorded in the Manchester Children's Tumour Registry from 1954 to 1989 were studied. After review of case notes, X-rays, and health surveys the clinical outcome and incidence of congenital anomaly was determined. A previously unreported association with Rubinstein Taybi syndrome was found. Evidence of a genetic syndrome or congenital anomaly was found in 6.4%. These figures provide further evidence of the higher-than-expected incidence of congenital abnormalities.
Affiliation:
Department of Cancer Genetics, Paterson Institute for Cancer Research, Manchester, England.
Citation:
Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma. 1993, 21 (6):433-4 Med. Pediatr. Oncol.
Journal:
Medical and Pediatric Oncology
Issue Date:
1993
URI:
http://hdl.handle.net/10541/99959
DOI:
10.1002/mpo.2950210608
PubMed ID:
8515724
Type:
Article
Language:
en
ISSN:
0098-1532
Appears in Collections:
All Christie Publications ; All Paterson Institute for Cancer Research

Full metadata record

DC FieldValue Language
dc.contributor.authorEvans, D Gareth Ren
dc.contributor.authorBurnell, Liza Den
dc.contributor.authorCampbell, Ren
dc.contributor.authorGattamaneni, Raoen
dc.contributor.authorBirch, Jillian Men
dc.date.accessioned2010-05-28T11:50:43Z-
dc.date.available2010-05-28T11:50:43Z-
dc.date.issued1993-
dc.identifier.citationCongenital anomalies and genetic syndromes in 173 cases of medulloblastoma. 1993, 21 (6):433-4 Med. Pediatr. Oncol.en
dc.identifier.issn0098-1532-
dc.identifier.pmid8515724-
dc.identifier.doi10.1002/mpo.2950210608-
dc.identifier.urihttp://hdl.handle.net/10541/99959-
dc.description.abstractOne hundred seventy-three consecutive cases of medulloblastoma recorded in the Manchester Children's Tumour Registry from 1954 to 1989 were studied. After review of case notes, X-rays, and health surveys the clinical outcome and incidence of congenital anomaly was determined. A previously unreported association with Rubinstein Taybi syndrome was found. Evidence of a genetic syndrome or congenital anomaly was found in 6.4%. These figures provide further evidence of the higher-than-expected incidence of congenital abnormalities.en
dc.language.isoenen
dc.subjectCerebellar Canceren
dc.subject.meshAdolescent-
dc.subject.meshCerebellar Neoplasms-
dc.subject.meshChild-
dc.subject.meshChild, Preschool-
dc.subject.meshCongenital Abnormalities-
dc.subject.meshEngland-
dc.subject.meshFemale-
dc.subject.meshHumans-
dc.subject.meshIncidence-
dc.subject.meshInfant-
dc.subject.meshMale-
dc.subject.meshMedulloblastoma-
dc.subject.meshRegistries-
dc.subject.meshSyndrome-
dc.titleCongenital anomalies and genetic syndromes in 173 cases of medulloblastoma.en
dc.typeArticleen
dc.contributor.departmentDepartment of Cancer Genetics, Paterson Institute for Cancer Research, Manchester, England.en
dc.identifier.journalMedical and Pediatric Oncologyen

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