Related Experiment Video
Updated: Aug 24, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
[Myasthenia gravis in children: clinical study of 77 patients]
Shui-zhen Zhou1, Wen-hui Li, Dao-kai Sun
1Department of Neurology, Children's Hospital, Fudan University, Shanghai 200032, China.
Insights
Pediatric myasthenia gravis (MG) shows earlier onset and increased Type II cases. Monitoring serology is crucial as seronegative patients can become positive, and steroids are effective treatments for childhood MG.
Area of Science:
- Pediatric Neurology
- Immunology
Background:
- Myasthenia Gravis (MG) is a rare autoimmune disorder affecting neuromuscular junctions.
- Understanding pediatric MG clinical characteristics and antibody status is vital for diagnosis and management.
Purpose of the Study:
- To investigate the clinical features of myasthenia gravis (MG) in children.
- To analyze changes in acetylcholine receptor antibody (AchR-Ab)-seronegative (SNMG) and seropositive (SPMG) pediatric MG patients.
Main Methods:
- A retrospective analysis of 77 pediatric MG patients diagnosed between 1992 and 2002.
- Clinical data, serological markers (AchR-Ab, PremRab, Tintinab), immunological cell counts, imaging (CT), and electromyography (EMG) were assessed.
Main Results:
- Early onset (before 3 years) was common, with extraocular muscles frequently affected. 35% were initially AchR-Ab positive. Notably, 60% of initially seronegative MG patients (SNMG) converted to seropositive (SPMG) upon follow-up.
- Abnormalities in CD cells (CD4+, CD3+, CD8+) were observed in 85% of cases. Thymus abnormalities, including hyperplasia and thymoma, were found in 42% and 4% of patients, respectively.
- Electromyography (EMG) showed abnormalities in 50% of cases. Treatment with anticholinesterase drugs and steroids generally led to good prognosis.
Conclusions:
- Pediatric MG incidence is rising, with a trend towards younger age of onset and increased Type II classifications.
- Regular serological monitoring is essential as SNMG patients can seroconvert to SPMG.
- Corticosteroids, particularly methylprednisolone, are effective and safe for treating pediatric MG, with fewer side effects compared to oral prednisone.
Objective:
To study the clinical characteristics of myasthenia gravis (MG) in children and the changes in AchR-Ab-seronegative (SNMG) MG and AchR-Ab-seropositive MG (SPMG) patients.
Methods:
The study was done on 77 MG patients who were diagnosed at The Pediatric Hospital, Fudan University from 1992 to 2002. This clinical trial was a non-randomized, controlled open study.
Results:
(1) The age of onset ranged from 3 months to 16 years, and the most common ages of onset were before 3 years; 32 cases were males and 45 females. The extraocular muscles were more frequently involved. According to the modified Osserman's criteria, 54 patients (70%) were classified as type I, 21 cases (27%) as type II and 2 cases (3%) as type III. (2) Eighteen of 55 cases (35%) were positive for anti-acetylcholine receptor antibodies (AchRab) and 16 of 55 cases (31%) were positive for acetylcholine premembrane receptor antibody (PremRab) on the initial examination. The clinical state of the patient during the examination did not show any clear correlation with the level of these antibodies. There was no significant difference between clinical type and AchRab positive rate among the three groups. Two of 18 patients (11%) were positive for thymoma associated antibody (Tintinab). The serological test on follow-up showed that 6 of 10 SNMG cases (60%) turned to be SPMG. In 85% of the cases the results of CD cells examination was abnormal, most of them showed reduced levels of CD4(+) or CD3(+) and CD8(+). (3) The thymus proliferation was found in 22 patients (42%) by CT and changes of thymoma were found in 2 cases (4%) and were confirmed by operation. (4) In 50% of the cases the electromyography (EMG) was abnormal. (5) After anticholinesterase drugs and steroids treatment the prognosis of patients with MG was usually good.
Conclusions:
MG in our children's hospital has increased, the age of onset became younger, and type II MG cases increased. Seronegative patients could turn positive, so monitoring the patient's serology is helpful for finding more SPMG cases. Steroids have been proven effective and safe in treatment of MG in children. Patients in methylprednisolone group experienced less side effects of steroid therapy than group treated with oral prednisone.
Related Concept Videos
Myasthenia Gravis: Diagnostic Tests
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
Myasthenia Gravis: Overview and Treatment
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which leads...
Myasthenia Gravis ll: Pathophysiology
Disorders of the Skeletal Muscle
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
Chemical Synapses
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Chemical Synapses
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...