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Updated: May 26, 2026

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Low-Cost Gait Analysis for Behavioral Phenotyping of Mouse Models of Neuromuscular Disease
Published on: July 18, 2019
Ring chromosome 21 in the differential diagnosis of waddling gait
Mutluay Arslan1, Uluç Yiş, Sebahattin Vurucu
1Gülhane Military Medical School, Department of Pediatrics, Division of Child Neurology, Etlik, Ankara, Turkey. mutluayarslan@yahoo.com
Brain & Development
|January 3, 2012
Abstract:
Ring chromosome 21 syndrome is a rare clinical condition. Most of the patients have a recognizable phenotype and multisystem involvement is described. Structural neurologic anomalies have also been described, but waddling gait due to lower motor neuron involvement has not been previously reported in association with ring 21.
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