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PMID: 7747773 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Tumors in Rubinstein-Taybi syndrome.

American journal of medical genetics ·Vol. 56 ·No. 1 ·1995-03-13 ·Pages 112-5

Miller RW, Rubinstein JH

Abstract

The 14 tumors reported in Rubinstein-Taybi syndrome since 1989, when added to the 22 previously reported, are beginning to show a pattern of neural and developmental tumors, especially of the head, which is malformed in the syndrome. Among the neoplasms were 12 of the nervous system: 2 each of oligodendroglioma, medulloblastoma, neuroblastoma, and benign meningioma, a pheochromocytoma, and 3 other benign tumors; 2 of nasopharyngeal rhabdomyosarcoma; and 1 each of leiomyosarcoma, seminoma, and embryonal carcinoma. Among the other benign tumors were an odontoma, a choristoma, a dermoid cyst, and 2 pilomatrixomas.

MeSH Terms
Adolescent Adult Child Child, Preschool Female Head and Neck Neoplasms/complications Humans Infant Infant, Newborn Male Middle Aged Neoplasms/complications Neoplasms, Germ Cell and Embryonal/complications Neoplasms, Nerve Tissue/complications Nervous System Neoplasms/complications Rubinstein-Taybi Syndrome/complications
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Miller R W
Clinical Epidemiology Branch, National Cancer Institute, Bethesda, Maryland 20892-7360, USA.
Rubinstein J H
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1995-03-13
Pages
112-5
Language
English
Region
United States
NLM ID
7708900
Subset
IM
Grants
PHS HHS · MCJ-399156-04-1 · United States
Corrections
CommentIn
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