Literature DB >> 4061768

Abnormal breathing in the Rett syndrome.

E Lugaresi, F Cirignotta, P Montagna.   

Abstract

Four girls affected with the Rett syndrome showed stereotyped hand movements and psychomotor regression beginning in the first or second year of life after initially normal development, with total loss of language, a severe gait, and chewing and swallowing disturbances. Breathing during active wakefulness was abnormal, with clusters of arrhythmic, tachypneic and irregular respiratory acts, intermixed with prolonged apneic episodes causing cyanosis and even fainting. On the other hand, breathing was regular during both NREM and REM sleep stages. Breathing impairment in the Rett syndrome is characterized by an inability to maintain normal respiratory patterns during wakefulness, and represents a functional disturbance of the behavioral control of breathing, which occurs during active wakefulness.

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Year:  1985        PMID: 4061768     DOI: 10.1016/s0387-7604(85)80039-5

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  16 in total

Review 1.  Rett syndrome and MeCP2: linking epigenetics and neuronal function.

Authors:  Mona D Shahbazian; Huda Y Zoghbi
Journal:  Am J Hum Genet       Date:  2002-11-19       Impact factor: 11.025

2.  The course of awake breathing disturbances across the lifespan in Rett syndrome.

Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Gamze Kilic Berkmen; Jana Drummond; Elizabeth Aronoff; Jennifer Harris; Jane B Lane; Walter E Kaufmann; Kathleen J Motil; Daniel G Glaze; Steven A Skinner; Alan K Percy
Journal:  Brain Dev       Date:  2018-04-12       Impact factor: 1.961

3.  Anaesthesia and Rett syndrome: a case report.

Authors:  D Maguire; C Bachman
Journal:  Can J Anaesth       Date:  1989-07       Impact factor: 5.063

Review 4.  Rett Syndrome: Reaching for Clinical Trials.

Authors:  Lucas Pozzo-Miller; Sandipan Pati; Alan K Percy
Journal:  Neurotherapeutics       Date:  2015-07       Impact factor: 7.620

5.  Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome.

Authors:  P F Giampietro; D B Schowalter; S Merchant; L R Campbell; T Swink; B B Roa
Journal:  Childs Nerv Syst       Date:  2005-05-05       Impact factor: 1.475

6.  Habituation without NMDA Receptor-Dependent Desensitization of Hering-Breuer Apnea Reflex in a Mecp2 Mutant Mouse Model of Rett Syndrome.

Authors:  Gang Song; Chung Tin; Emanuela Giacometti; Chi-Sang Poon
Journal:  Front Integr Neurosci       Date:  2011-05-02

7.  Hyperventilation in the awake state: potentially treatable component of Rett syndrome.

Authors:  D P Southall; A M Kerr; E Tirosh; P Amos; M H Lang; J B Stephenson
Journal:  Arch Dis Child       Date:  1988-09       Impact factor: 3.791

8.  Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.

Authors:  J M Bissonnette; L R Schaevitz; S J Knopp; Z Zhou
Journal:  Neuroscience       Date:  2014-03-10       Impact factor: 3.590

9.  Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome.

Authors:  Jun Ren; Xiuqing Ding; Gregory D Funk; John J Greer
Journal:  J Neurosci       Date:  2012-11-28       Impact factor: 6.167

10.  Deficiency of GABAergic synaptic inhibition in the Kölliker-Fuse area underlies respiratory dysrhythmia in a mouse model of Rett syndrome.

Authors:  Ana Paula Abdala; Marie A Toward; Mathias Dutschmann; John M Bissonnette; Julian F R Paton
Journal:  J Physiol       Date:  2015-12-14       Impact factor: 5.182

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