Ring chromosome 21 in the differential diagnosis of waddling gait.

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. Copyright © 2011 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Citation

Mutluay Arslan, Uluç Yiş, Sebahattin Vurucu, Yusuf Tunca, Bülent Unay, Rıdvan Akin. Ring chromosome 21 in the differential diagnosis of waddling gait. Brain & development. 2012 Oct;34(9):792-5

Mesh Tags

PMID: 22209335

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