Literature DB >> 11714563

Episodic cervical dystonia associated with gastro-oesophageal reflux. A case of adult-onset Sandifer syndrome.

M Shahnawaz1, L R van der Westhuizen, R F Gledhill.   

Abstract

Sandifer syndrome is a dystonic movement disorder described in children with severe gastro-oesophageal reflux. We now report a patient who had the features of Sandifer syndrome first developing in adult life. Onset of dystonic episodes followed closely the occurrence of a Bell's palsy, while symptoms of peptic oesophagitis had been present for several months beforehand. Successful symptomatic treatment of gastro-oesophageal reflux was accompanied by cessation of the dystonic episodes. Possible pathophysiological mechanisms of the abnormal movements in Sandifer syndrome are discussed.

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Year:  2001        PMID: 11714563     DOI: 10.1016/s0303-8467(01)00145-7

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  5 in total

1.  A chronic case of adult-onset Sandifer syndrome.

Authors:  Abdul Qayyum Rana; Muhammad Saad Yousuf; Saliman Joian
Journal:  Neurol Sci       Date:  2012-03-13       Impact factor: 3.307

Review 2.  Diagnosis and management of acute movement disorders.

Authors:  D Dressler; R Benecke
Journal:  J Neurol       Date:  2005-10-10       Impact factor: 4.849

Review 3.  Sandifer syndrome posturing: relation to abdominal wall contractions, gastroesophageal reflux, and fundoplication.

Authors:  Eric A Frankel; Theresa M Shalaby; Susan R Orenstein
Journal:  Dig Dis Sci       Date:  2006-04       Impact factor: 3.199

4.  Effects of Osteopathic Visceral Treatment in Patients with Gastroesophageal Reflux: A Randomized Controlled Trial.

Authors:  Nuria Eguaras; Elena Sonsoles Rodríguez-López; Olga Lopez-Dicastillo; M Ángeles Franco-Sierra; François Ricard; Ángel Oliva-Pascual-Vaca
Journal:  J Clin Med       Date:  2019-10-19       Impact factor: 4.241

5.  Paroxysmal head drops with ataxia-like symptoms presenting as Sandifer syndrome in a 3-year old girl.

Authors:  Abubakar Sharif; Lucinda Carr; Efstratios Saliakellis; Himadri Chakraborty
Journal:  BMJ Case Rep       Date:  2020-03-04
  5 in total

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