Literature DB >> 16484061

A new syndrome with quadrupedal gait, primitive speech, and severe mental retardation as a live model for human evolution.

Uner Tan1.   

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.

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Year:  2006        PMID: 16484061     DOI: 10.1080/00207450500455330

Source DB:  PubMed          Journal:  Int J Neurosci        ISSN: 0020-7454            Impact factor:   2.292


  17 in total

1.  The very low density lipoprotein receptor-associated pontocerebellar hypoplasia and dysmorphic features in three Turkish patients.

Authors:  Fatma Mujgan Sonmez; Joseph G Gleeson; Figen Celep; Sibel Kul
Journal:  J Child Neurol       Date:  2012-04-24       Impact factor: 1.987

2.  Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion.

Authors:  Onur Emre Onat; Suleyman Gulsuner; Kaya Bilguvar; Ayse Nazli Basak; Haluk Topaloglu; Meliha Tan; Uner Tan; Murat Gunel; Tayfun Ozcelik
Journal:  Eur J Hum Genet       Date:  2012-08-15       Impact factor: 4.246

3.  Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred.

Authors:  Suleyman Gulsuner; Ayse Begum Tekinay; Katja Doerschner; Huseyin Boyaci; Kaya Bilguvar; Hilal Unal; Aslihan Ors; O Emre Onat; Ergin Atalar; A Nazli Basak; Haluk Topaloglu; Tulay Kansu; Meliha Tan; Uner Tan; Murat Gunel; Tayfun Ozcelik
Journal:  Genome Res       Date:  2011-09-01       Impact factor: 9.043

4.  Two Indian Families with Quadrupedal Locomotion Resembling Uner Tan Syndrome: A Video Document.

Authors:  Gurusidheshwar Wali
Journal:  Mov Disord Clin Pract       Date:  2016-06-06

5.  ATP8A2-related disorders as recessive cerebellar ataxia.

Authors:  Claire Guissart; Alexander N Harrison; Mehdi Benkirane; Ibrahim Oncel; Elif Acar Arslan; Anna K Chassevent; Kristin Baraῆano; Lise Larrieu; Maria Iascone; Romano Tenconi; Mireille Claustres; Nesibe Eroglu-Ertugrul; Patrick Calvas; Haluk Topaloglu; Robert S Molday; Michel Koenig
Journal:  J Neurol       Date:  2019-10-14       Impact factor: 4.849

6.  Use it or lose it? Effects of age, experience, and disuse on crawling.

Authors:  Whitney G Cole; Beatrix Vereijken; Jesse W Young; Scott R Robinson; Karen E Adolph
Journal:  Dev Psychobiol       Date:  2018-11-16       Impact factor: 3.038

Review 7.  The neural control of interlimb coordination during mammalian locomotion.

Authors:  Alain Frigon
Journal:  J Neurophysiol       Date:  2017-03-15       Impact factor: 2.714

8.  Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Authors:  Luis E Kolb; Zulfikar Arlier; Cengiz Yalcinkaya; Ali K Ozturk; Jennifer A Moliterno; Ozdem Erturk; Fatih Bayrakli; Baris Korkmaz; Michael L DiLuna; Katsuhito Yasuno; Kaya Bilguvar; Tayfun Ozcelik; Beyhan Tuysuz; Matthew W State; Murat Gunel
Journal:  Neurogenetics       Date:  2010-01-15       Impact factor: 2.660

9.  Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans.

Authors:  Tayfun Ozcelik; Nurten Akarsu; Elif Uz; Safak Caglayan; Suleyman Gulsuner; Onur Emre Onat; Meliha Tan; Uner Tan
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-07       Impact factor: 11.205

10.  Central pattern generator for locomotion: anatomical, physiological, and pathophysiological considerations.

Authors:  Pierre A Guertin
Journal:  Front Neurol       Date:  2013-02-08       Impact factor: 4.003

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