Achalasia is an esophageal motility disorder characterized by failure of lower esophageal sphincter (LES) relaxation and is rare in children. The most common symptoms are vomiting, dysphagia, regurgitation, and weight loss. Definitive diagnosis is made with barium swallow study and esophageal manometry. In adults, endoscopic biopsy is recommended to exclude malignancy however; it is not as often indicated in children. Medical management often fails resulting in recurrent symptoms and the ultimate definitive treatment is surgical. Laparoscopic Heller myotomy with or without an anti-reflux procedure is the treatment of choice and has become standard of care for children with achalasia. Peroral endoscopic myotomy is a novel therapy utilized wi...
Achalasia is an extremely rare pathology in children. Peroral endoscopic myotomy (POEM) is the gold ...
© 2016 Elsevier Inc. Background Surgical management of esophageal achalasia (EA) in children has tra...
The Authors present a retrospective review of their record of cases, characterized by 4 cases of ach...
Achalasia is a rare esophageal motility disorder. Much of the literature is based on the adult popul...
Achalasia is a rare neurogenic motility disorder of the esophagus, occurring in approximately 0.11 c...
OBJECTIVES: Pediatric achalasia is a rare neurodegenerative disorder of the esophagus that requires ...
Introduction: Achalasia is a primary oesophageal motility disorder with unknown aetiology. The aim o...
Achalasia was a condition marked by peristaltic movement absent in lower esophageal sphincter and se...
Achalasia is a primary motor disorder of the esophagus, in which esophageal emptying is impaired. Di...
Purpose: The optimal management of achalasia in children and adolescents remains unclear. The aim of...
Achalasia was a condition marked by peristaltic movement absent in lower esophageal sphincter and se...
Introduction Primary achalasia is an idiopathic motility disorder of the esophagus characterized by ...
Esophageal achalasia (EA) is a rare esophageal motility disorder in children. Laparoscopic Heller my...
Achalasia is an esophageal motility disorder of unknown cause, characterized by aperistalsis of the ...
Background: In spite of the introduction of peroral endoscopic myotomy (POEM), Heller myotomy (HM) r...
Achalasia is an extremely rare pathology in children. Peroral endoscopic myotomy (POEM) is the gold ...
© 2016 Elsevier Inc. Background Surgical management of esophageal achalasia (EA) in children has tra...
The Authors present a retrospective review of their record of cases, characterized by 4 cases of ach...
Achalasia is a rare esophageal motility disorder. Much of the literature is based on the adult popul...
Achalasia is a rare neurogenic motility disorder of the esophagus, occurring in approximately 0.11 c...
OBJECTIVES: Pediatric achalasia is a rare neurodegenerative disorder of the esophagus that requires ...
Introduction: Achalasia is a primary oesophageal motility disorder with unknown aetiology. The aim o...
Achalasia was a condition marked by peristaltic movement absent in lower esophageal sphincter and se...
Achalasia is a primary motor disorder of the esophagus, in which esophageal emptying is impaired. Di...
Purpose: The optimal management of achalasia in children and adolescents remains unclear. The aim of...
Achalasia was a condition marked by peristaltic movement absent in lower esophageal sphincter and se...
Introduction Primary achalasia is an idiopathic motility disorder of the esophagus characterized by ...
Esophageal achalasia (EA) is a rare esophageal motility disorder in children. Laparoscopic Heller my...
Achalasia is an esophageal motility disorder of unknown cause, characterized by aperistalsis of the ...
Background: In spite of the introduction of peroral endoscopic myotomy (POEM), Heller myotomy (HM) r...
Achalasia is an extremely rare pathology in children. Peroral endoscopic myotomy (POEM) is the gold ...
© 2016 Elsevier Inc. Background Surgical management of esophageal achalasia (EA) in children has tra...
The Authors present a retrospective review of their record of cases, characterized by 4 cases of ach...