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Updated: Jun 21, 2026

Whole Body Vibration Methods with Survivors of Polio
Published on: October 17, 2018
Pediatric monomelic amyotrophy: evidence for poliomyelitis in vulnerable populations
Hugh J McMillan1, Basil T Darras, Peter B Kang
1Department of Neurology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts, USA.
Insights
Pediatric monomelic amyotrophy is difficult to diagnose, especially in children with limited medical history. This study suggests polio-related viruses as a likely cause for this rare condition.
Area of Science:
- Neurology
- Pediatric Neurology
- Infectious Diseases
Background:
- Pediatric monomelic amyotrophy (PMA) presents diagnostic challenges, particularly in adopted or immigrant children lacking medical history.
- Monomelic amyotrophy (PMA) is a rare neuromuscular disorder characterized by muscle wasting in a specific limb.
Purpose of the Study:
- To investigate the potential causes of pediatric monomelic amyotrophy (PMA) in children with limited medical history.
- To analyze clinical and electrophysiological findings in pediatric patients with unilateral or asymmetric motor neuronopathy.
Main Methods:
- Clinical data collection from 11 pediatric patients diagnosed with monomelic amyotrophy (PMA).
- Electrophysiological studies to assess motor neuron function and identify patterns of neuropathy.
- Review of medical histories, focusing on potential infectious etiologies.
Main Results:
- All 11 children exhibited electrophysiological evidence of unilateral or profoundly asymmetric motor neuronopathy.
- The findings were most consistent with prior infections from wildtype poliovirus, "polio-like" viruses, or vaccine-associated paralytic poliomyelitis.
- Diagnostic challenges were exacerbated by the lack of comprehensive medical histories in immigrant or adopted children.
Conclusions:
- Polio-related viral infections are a significant potential cause of pediatric monomelic amyotrophy (PMA).
- Electrophysiological evidence of asymmetric motor neuronopathy supports a polio-like etiology in these cases.
- Further investigation is needed to confirm the specific viral agents responsible for PMA in this population.
Abstract:
Pediatric monomelic amyotrophy may present a diagnostic challenge. This is particularly true for immigrant or adopted children who have little or no available medical history. We present clinical and electrophysiological data from 11 children with monomelic amyotrophy who had electrophysiological evidence of a unilateral or profoundly asymmetric motor neuronopathy. The cause of amyotrophy in each case is most consistent with prior: (1) wildtype poliovirus myelitis; (2) "polio-like" virus myelitis, or (3) vaccine associated paralytic poliomyelitis.
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