Open Journal of Pediatrics

Volume 9, Issue 3 (September 2019)

ISSN Print: 2160-8741   ISSN Online: 2160-8776

Google-based Impact Factor: 0.45  Citations  

Sandifer’s Syndrome in a 3-Month-Old Male Infant: A Case Report

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DOI: 10.4236/ojped.2019.93022    966 Downloads   10,361 Views  

ABSTRACT

Background: Sandifer syndrome (SS) is the association of gastroesophageal reflux disease (GERD) with neurological manifestations (spastic torticollis and paroxysmal dystonic postures with arching of the back and rigid opisthotonic posturing. Case presentation: A 3-month-old male infant presented to our emergency department with torticollis and dystonic episodes for two months associated with vomiting. These movements were observed during or just after feeding. Since the patient developed regurgitations with torticollis and dystonic episodes with arching of the back and rigid opisthotonic posturing. The electroencephalogram was normal. Barium swallow/meal examination revealed GERD without evidence of hiatus hernia. Apgar scores were 7 at 1 min and 9 at 5 min. Conclusion: Early recognition and treatment of GERD in patients with Sandifer syndrome enhance the success of medical management and contributes to improved quality of life for patients with brain damage. The paroxysmal dystonic behaviors were dramatically disappeared completely after medical management in this patient.

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Basal, A. , Aldirawi, A. and Abuzerr, S. (2019) Sandifer’s Syndrome in a 3-Month-Old Male Infant: A Case Report. Open Journal of Pediatrics, 9, 232-238. doi: 10.4236/ojped.2019.93022.

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