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DOI: 10.1055/s-0030-1262862
© Georg Thieme Verlag KG Stuttgart · New York
Hypertonic Upper Esophageal Sphincter in Down's Syndrome: A Case Report
Publication History
Publication Date:
11 October 2010 (online)

Introduction
Down's syndrome (DS) (a genetically determined disorder caused by trisomy 21) may be associated with a variety of dysfunctions that can affect any organ and system. Esophageal atresia and tracheoesophageal fistula are the most recognized esophageal disorders in DS [1] but there are reported cases of the coexistence of Down's syndrome and esophageal achalasia [2] [3]. In these studies achalasia is generally characterized by the lack of peristaltic contractions of the esophageal body, increased lower esophageal sphincter (LES) pressure, and impaired LES relaxation during swallowing. Abnormalities in esophageal motility can result in swallowing difficulties, heartburn and regurgitation.
We report on a child with DS and cricopharyngeal (CP) dysfunction due to hypertonic upper esophageal sphincter (UES) successfully treated with surgery.
References
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- 4 Rosenbek JC, Robbins J, Roecker EV. et al . A Penetration-Aspiration Scale. Dysphagia. 1996; 11 93-98
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Correspondence
Dr. Elena Carraro
University of Padova
Department of Rehabilitation
Via Giustiniani 2
35128 Padova
Italy
Phone: +39 0498 218 471
Fax: +39 0498 211 796
Email: e_carraro@yahoo.it