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 Andrews, P. I.
Right arrow Articles by Sanders, D. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Andrews, P. I.
Right arrow Articles by Sanders, D. B.
NEUROLOGY 1994;44:1208
© 1994 American Academy of Neurology

Race, sex, and puberty influence onset, severity, and outcome in juvenile myasthenia gravis

P. Ian Andrews, FRACP, Janice M. Massey, MD, James F. Howard, Jr., MD and Donald B. Sanders, MD

Departments of Pediatrics (Dr. Andrews) and Medicine (Drs. Massey and Sanders), Duke University Medical Center, Durham, and the Department of Neurology (Dr. Howard), University of North Carolina at Chapel Hill, Chapel Hill, NC.

We assessed the influence of race, sex, and puberty upon clinical features and outcome in 115 patients with autoimmune juvenile myasthenia gravis (JMG). These demographic variables influenced not only disease incidence but also disease severity, response to therapy, and outcome, despite comparable therapeutic strategies. Among white patients, those with prepubertal onset had low incidence and equal sex ratio; the incidence in females increased during and after puberty; males had lesser disease severity than females during and after puberty (p < 0.05); spontaneous remissions were most frequent (44%, p = 0.001) and persistence of active JMG for more than 10 years was least frequent (p = 0.05) in patients with prepubertal onset; remissions were more frequent after early than late thymectomy (p = 0.03); and final disease severity was less after early than late thymectomy. Black patients had similar incidence, disease severity, and sex ratio (F:M = 2:1) with pre-, peri-, or postpubertal disease onset; infrequent spontaneous or treatment-induced remissions; and the same final disease severity after early or late thymectomy. These observations imply that race and sex hormones modify the clinical features and outcome of JMG; spontaneous remissions are common in white patients with prepubertal disease onset; early thymectomy may be more beneficial than late thymectomy in white patients; and the role of thymectomy in the youngest patients is uncertain. We suggest that demographic factors should be considered when evaluating past and future therapeutic strategies for JMG.

Address correspondence and reprint requests to Dr. P. Ian Andrews, Division of Pediatric Neurology, Box 3533, Duke University Medical Center, Durham, NC 27710.

Received October 19, 1993. Accepted in final form January 20, 1994.




This article has been cited by other articles:


Home page
Eur. J. Cardiothorac. Surg.Home page
M. Essa, Y. El-Medany, W. Hajjar, Z. Hariri, F. Al-Mulhim, M. Salih, M. Ashour, and K. Al-Kattan
Maximal thymectomy in children with myasthenia gravis
Eur. J. Cardiothorac. Surg., August 1, 2003; 24(2): 187 - 191.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
G. Haliloglu, B. Anlar, S. Aysun, M. Topcu, H. Topaloglu, G. Turanli, and D. Yalnizoglu
Gender Prevalence in Childhood Multiple Sclerosis and Myasthenia Gravis
J Child Neurol, May 1, 2002; 17(5): 390 - 392.
[Abstract] [PDF]


Home page
J Child NeurolHome page
H. K. Kolski, P. C.W. Kim, and J. Vajsar
Video-Assisted Thoracoscopic Thymectomy in Juvenile Myasthenia Gravis
J Child Neurol, August 1, 2001; 16(8): 569 - 573.
[Abstract] [PDF]


Home page
NeurologyHome page
A. Jaretzki III, R. J. Barohn, R. M. Ernstoff, H. J. Kaminski, J. C. Keesey, A. S. Penn, and D. B. Sanders
Myasthenia gravis: Recommendations for clinical research standards
Neurology, July 12, 2000; 55(1): 16 - 23.
[Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
A. Jaretzki III, R. J. Barohn, R. M. Ernstoff, H. J. Kaminski, J. C. Keesey, A. S. Penn, and D. B. Sanders
Myasthenia gravis: recommendations for clinical research standards
Ann. Thorac. Surg., July 1, 2000; 70(1): 327 - 334.
[Full Text] [PDF]


Home page
J Child NeurolHome page
J. S. Janas and R. J. Barohn
A Clinical Approach to the Congenital Myasthenic Syndromes
J Child Neurol, March 1, 1995; 10(2): 168 - 169.
[PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1994 by AAN Enterprises, Inc.