2017
DOI: 10.4172/2472-1115.1000124
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Pediatric Comorbidities and Medical Complications Identified in Children with Down Syndrome

Abstract: Objective: Children with Down syndrome (DS) have an increased risk of neonatal complications and comorbidities compared to the general population; however, the incidence, optimal screening intervals and outcomes in this population are uncertain. The purpose of this study is to phenotypically define this population of children with DS using a large multi-age and ethnic sample and current American Academy of Pediatrics (AAP) Guidelines testing practices.Method: This is a retrospective review of a large cohort of… Show more

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Cited by 9 publications
(10 citation statements)
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“…GI abnormalities occur in approximately 12% of patients. 11 Duodenal atresia or stenosis, Hirschsprung disease, tracheoesophageal fistula, Meckel diverticulum, imperforate anus, and omphalocele are observed. Gastroesophageal reflux is commonly seen in children with Down syndrome and can be severe enough to result in aspiration of stomach contents, resulting in respiratory symptoms such as persistent coughing, wheezing, and pneumonia.…”
Section: Discussionmentioning
confidence: 99%
“…GI abnormalities occur in approximately 12% of patients. 11 Duodenal atresia or stenosis, Hirschsprung disease, tracheoesophageal fistula, Meckel diverticulum, imperforate anus, and omphalocele are observed. Gastroesophageal reflux is commonly seen in children with Down syndrome and can be severe enough to result in aspiration of stomach contents, resulting in respiratory symptoms such as persistent coughing, wheezing, and pneumonia.…”
Section: Discussionmentioning
confidence: 99%
“…Data results indicate that clinic patients capture approximately 50.3% of the state of Colorado's population of children with DS and provide support of a population‐based representation (Hickey et al . ). The second paediatric hospital has similar demographic representation of the community.…”
Section: Methodsmentioning
confidence: 97%
“…Results indicate that SCDS clinic patients capture approximately 50.3% of the state of Colorado’s population of children with Down syndrome and provides support for a population-based representation. 26 Because we tested infantile spasms diagnosis differences separately for each of the 5 medical comorbidities and complications, we used the Benjamini and Hochberg false discovery rate to control for potential Type I errors. 27 Fisher’s exact tests were conducted between ACTH, vigabatrin, oral steroids, and other treatments with (1) regression of skills at spasms onset, (2) cessation of spasms at 2 weeks (n = 32), and (3) cessation of spasms at 3 months (n = 34).…”
Section: Methodsmentioning
confidence: 99%