Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kaufman, D. K.
Right arrow Articles by Michels, V. V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kaufman, D. K.
Right arrow Articles by Michels, V. V.
NEUROLOGY 1993;43:1728
© 1993 American Academy of Neurology

A familial syndrome with cutaneous malignant melanoma and cerebral astrocytoma

David K. Kaufman, MD, David W. Kimmel, MD, Joseph E. Parisi, MD and Virginia V. Michels, MD

Departments of Neurology (Drs. Kaufman and Kimmel), Laboratory Medicine and Pathology (Dr. Parisi), and Medical Genetics (Dr. Michels), Mayo Clinic and Mayo Foundation, Rochester, MN.

We describe a family in which cutaneous malignant melanoma or cerebral astrocytoma, or both, developed in eight members over three generations. Other malignancies also occurred with a lesser frequency. In two patients with both malignant melanoma and astrocytoma, the brain tumor followed the diagnosis of melanoma by a period of 2 and 10 years and was the primary cause of morbidity and mortality. The findings in this family may represent a newly described genetic disorder.

Address correspondence and reprint requests to Dr. David Kimmel, Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905.

Supported in part by research grant CA50905 from the National Cancer Institute.

Received October 22, 1992. Accepted for publication in final form January 22, 1993.




This article has been cited by other articles:


Home page
Cancer Res.Home page
E. Pasmant, I. Laurendeau, D. Heron, M. Vidaud, D. Vidaud, and I. Bieche
Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL, an Antisense Noncoding RNA Whose Expression Coclusters with ARF
Cancer Res., April 15, 2007; 67(8): 3963 - 3969.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
V P Collins
Brain tumours: classification and genes
J. Neurol. Neurosurg. Psychiatry, June 1, 2004; 75(suppl_2): ii2 - ii11.
[Full Text] [PDF]


Home page
Hum Mol GenetHome page
J. A. Randerson-Moor, M. Harland, S. Williams, D. Cuthbert-Heavens, E. Sheridan, J. Aveyard, K. Sibley, L. Whitaker, M. Knowles, J. Newton Bishop, et al.
A germline deletion of p14ARF but not CDKN2A in a melanoma-neural system tumour syndrome family
Hum. Mol. Genet., January 1, 2001; 10(1): 55 - 62.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
D. Dilworth, L. Liu, A. K. Stewart, J. R. Berenson, N. Lassam, and D. Hogg
Germline CDKN2A mutation implicated in predisposition to multiple myeloma
Blood, March 1, 2000; 95(5): 1869 - 1871.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
O. Hurko and T. T Provost
Neurology and the skin
J. Neurol. Neurosurg. Psychiatry, April 1, 1999; 66(4): 417 - 430.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1993 by AAN Enterprises, Inc.