Biomaterial Database

Colonic atresia presenting as neonatal bowel obstruction in cystic fibrosis. 2014

Tom S Yap, and Ashish Jiwane, and Yvonne Belessis, and Chee Y Ooi

*Department of Gastroenterology †Department of Pediatric Surgery ‡Department of Respiratory Medicine, Sydney Children's Hospital, Randwick, Australia.

UI	MeSH Term	Description	Entries
D007231	Infant, Newborn	An infant during the first 28 days after birth.	Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007409	Intestinal Atresia	Congenital obliteration of the lumen of the intestine, with the ILEUM involved in 50% of the cases and the JEJUNUM and DUODENUM following in frequency. It is the most frequent cause of INTESTINAL OBSTRUCTION in NEWBORNS. (From Stedman, 25th ed)	Atresia, Intestinal,Apple Peel Small Bowel Syndrome,Apple Peel Syndrome,Apple-Peel Intestinal Atresia,Congenital Intestinal Atresia,Familial Apple Peel Jejunal Atresia,Jejunal Atresia,Apple Peel Intestinal Atresia,Apple Peel Syndromes,Apple-Peel Intestinal Atresias,Atresia, Apple-Peel Intestinal,Atresia, Congenital Intestinal,Atresia, Jejunal,Atresias, Apple-Peel Intestinal,Atresias, Congenital Intestinal,Congenital Intestinal Atresias,Intestinal Atresia, Apple-Peel,Intestinal Atresia, Congenital,Intestinal Atresias, Apple-Peel,Intestinal Atresias, Congenital
D007415	Intestinal Obstruction	Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL.	Intestinal Obstructions,Obstruction, Intestinal
D003106	Colon	The segment of LARGE INTESTINE between the CECUM and the RECTUM. It includes the ASCENDING COLON; the TRANSVERSE COLON; the DESCENDING COLON; and the SIGMOID COLON.	Appendix Epiploica,Taenia Coli,Omental Appendices,Omental Appendix,Appendices, Omental,Appendix, Omental
D003550	Cystic Fibrosis	An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.	Mucoviscidosis,Cystic Fibrosis of Pancreas,Fibrocystic Disease of Pancreas,Pancreatic Cystic Fibrosis,Pulmonary Cystic Fibrosis,Cystic Fibrosis, Pancreatic,Cystic Fibrosis, Pulmonary,Fibrosis, Cystic,Pancreas Fibrocystic Disease,Pancreas Fibrocystic Diseases
D005183	Failure to Thrive	A condition of substandard growth or diminished capacity to maintain normal function.	Thrive, Failure to
D005260	Female		Females
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man