Warning: fopen(/home/virtual/pediatrics/journal/upload/ip_log/ip_log_2024-04.txt) [function.fopen]: failed to open stream: Permission denied in /home/virtual/pediatrics/journal/ip_info/view_data.php on line 82

Warning: fwrite(): supplied argument is not a valid stream resource in /home/virtual/pediatrics/journal/ip_info/view_data.php on line 83
A clinical study on Myasthenia gravis in childhood.

Journal of the Korean Pediatric Society 1985;28(2):154-159.
Published online February 28, 1985.
A clinical study on Myasthenia gravis in childhood.
Yong Seung Hwang, Hyo Seop Ahn, Sang Hyup Kim
Department of Pediatrics,College of Medicine,Seoul National University
소아기 중증근무력증에 대한 임상적 관찰
황용승, 안효섭, 김상협
서울대학교 의 과대학 소아과학교실
Abstract
Twenty-six cases of myasthenia gravis (MG) in childhood who were diagnosed and treated in the Department of Pediatrics, Seoul National University Hospital from January 1976 till October 1984 were reviewed clinically. Mean age of onset of MG was 5.4+3.6 years of age with the peak incidence at 2 years of age. Sexual difference was negligible as male to female ratio was 1.36 : 1. The most common initial clinical manifestation was ptosis noted in all cases, followed by external ophthalmoplegia in 34.6% of cases, weakness of legs in 19.2% and diplopia, dysphonia, weakness of arms in 15.4% respectively. According to the classification of MG by Osserman, ocular MG group I , was 18 cases (69%). There was no case associated with thymoma or other disease. Only anticholinesterase therapy were tried in 23 cases with improvement in 21 patient. Among them, five cases were in state of complete remission without drugs and nine cases were in remission with drugs. These findings suggest that MG in childhood has lower age of onset, is mostly ocular type and responds well to anticholinesterase therapy alone.
Key Words: Myasthenia gravis


METRICS Graph View
  • 878 View
  • 0 Download