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A NEW SYNDROME WITH QUADRUPEDAL GAIT, PRIMITIVE SPEECH, AND SEVERE MENTAL RETARDATION AS A LIVE MODEL FOR HUMAN EVOLUTION  Supplementary content is available for this

Author: Uner Tan a
Affiliation:   a Department of Physiology, Cukurova University Medical School, Adana, Turkey
DOI: 10.1080/00207450500455330
Publication Frequency: 12 issues per year
Published in: journal International Journal of Neuroscience, Volume 116, Issue 3 March 2006 , pages 361 - 369
Subject: Neuroscience;
Formats available: HTML (English) : PDF (English)
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Abstract

The author has discovered a new syndrome with quadrupedal gait, flexed head and body, primitive speech, severe mental retardation, and mild cerebellar signs with a disturbed conscious experience. This syndrome was exhibited by 5 of 19 children from a consanguineous family. The pedigree demonstrated a typical autosomal-recessive inheritance. The genetic nature of this syndrome suggests a backward stage in human evolution, which is most probably caused by a genetic mutation, rendering, in turn, the transition from quadrupedality to bipedality. This would then be consistent with theories of punctuated evolution. On the other hand, the extensor motor system causing a resistance of the body against the gravity may actually be subjected to evolutionary forces. This new syndrome may be used as a live model for human evolution.

An accompanying video clip for this article is available as a downloadable file accompanying the official online version of International Journal of Neuroscience. To access it, click on the issue link for 116(3), then select this article. A download option appears at the bottom of this abstract.
Keywords: erect posture; evolution; human quadrupedal gait
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