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 MD, T. A.
Right arrow Articles by Hejtmancik, J. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by MD, T. A.
Right arrow Articles by Hejtmancik, J. F.
NEUROLOGY 1992;42:1871
© 1992 American Academy of Neurology

Anticipation in myotonic dystrophy

I. Statistical verification based on clinical and haplotype findings

T. Ashizawa MD, C. J. Dunne, RN, BS, J. R. Dubel, PhD, M. B. Perryman, PhD, H. F. Epstein, MD, E. Boerwinkle PhD and J. F. Hejtmancik, MD, PhD

Departments of Neurology (Drs. Ashizawa, Dubel, and Epstein, and C.J. Dunne) and Medicine (Section of Cardiology) (Dr. Perryman), Baylor College of Medicine Center, Houston, TX Veterans Affairs Medical Center (Drs. Ashizawa and Dubel), Houston, TX, Genetic Centers (Dr. Boerwinkle), University of Texas Health Science Center, Houston, TX and National Eye Institute (Dr. Hejtmancik), National Institutes of Health, Bethesda, MD.

To determine whether anticipation in myotonic dystrophy (DM) is a true biologic phenomenon or an artifact of ascertainment bias, we studied 201 members of nine DM kindreds, including 67 individuals with the clinical diagnosis of DM. Of 49 parent-child pairs in which both the parents and the children were clinically affected, the onset of DM occurred in an earlier decade of life in the child than the parent in 44 pairs and in the same decade in five pairs (p < 0.001). To eliminate direct ascertainment bias, we excluded nine pairs involving the index patients. Indirect ascertainment bias due to incomplete penetrance was unlikely, since 55% of the children of DM parents had DM. Howeveip, by haplotype analysis of restriction fragment length polymorphisms, we diagnosed DM in one of the 42 asymptomatic children of affected parents and excluded DM in twenty-eight. We estimated that patients with early-onset DM would have produced an additional 25 DM children if they had normal fertility and nuptiality. Assuming that the expected age-of-onset distribution occurs without anticipation in these 25, only seven would have had the onset of DM earlier than their parents. With the corrected result, the child would have been affected earlier than the parent in 53 pairs, and the parent would have been affected at the same age as or earlier than the child in 13 pairs (p ≤ 0.001). Thus, the observed anticipation is unlikely to be totally attributable to ascertainment bias, suggesting the potential importance of biologic mechanisms.

Address correspondence and reprint requests to Dr. T. Ashizawa, Department of Neurology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030.

Supported by VA Merit Review (T.A.).

Received January 15, 1992. Accepted for publication in final form March 25, 1992




This article has been cited by other articles:


Home page
Endocr Relat CancerHome page
M Capezzone, S Marchisotta, S Cantara, G Busonero, L Brilli, K Pazaitou-Panayiotou, A F Carli, G Caruso, P Toti, S Capitani, et al.
Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity
Endocr. Relat. Cancer, December 1, 2008; 15(4): 1075 - 1081.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
S. Fokstuen, J. Myring, L. Meredith, D. Ravine, and P. S Harper
Eight years' experience of direct molecular testing for myotonic dystrophy in Wales
J. Med. Genet., December 1, 2001; 38 (12): e42 - e42.
[Full Text] [PDF]


Home page
Hum Mol GenetHome page
N. Sergeant, B. Sablonniere, S. Schraen-Maschke, A. Ghestem, C.-A. Maurage, A. Wattez, P. Vermersch, and A. Delacourte
Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1
Hum. Mol. Genet., September 1, 2001; 10(19): 2143 - 2155.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
C. Schneider, A. Ziegler, K. Ricker, T. Grimm, W. Kress, C. D. Reimers, H.-M. Meinck, K. Reiners, and K. V. Toyka
Proximal myotonic myopathy: Evidence for anticipation in families with linkage to chromosome 3q
Neurology, August 8, 2000; 55(3): 383 - 388.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. W. Bush, C. S. Taft, G. E. Meixell, and M. B. Perryman
Overexpression of Myotonic Dystrophy Kinase in BC(3)H1 Cells Induces the Skeletal Muscle Phenotype
J. Biol. Chem., January 5, 1996; 271(1): 548 - 552.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 by AAN Enterprises, Inc.