The adolescent child with short bowel syndrome: new onset of failure to thrive and need for increased nutritional supplementation

2010 ◽  
Vol 45 (6) ◽  
pp. 1280-1286 ◽  
Author(s):  
Eiichi A. Miyasaka ◽  
Pamela I. Brown ◽  
Shirley Kadoura ◽  
Mary Beth Harris ◽  
Daniel H. Teitelbaum
Keyword(s):  
Short Bowel Syndrome ◽  
Failure To Thrive ◽  
Nutritional Supplementation ◽  
Short Bowel ◽  
Adolescent Child ◽  
New Onset

scholarly journals Congenital Short Bowel Syndrome

2019 ◽  
Vol 18 (1) ◽  
pp. 35-37
Author(s):  
Amar Kumar Saha ◽  
Sheikh Sayidul Haque ◽  
Sunil Kumar Biswas ◽  
Md Barkot Ali
Keyword(s):  
Small Bowel ◽  
Parenteral Nutrition ◽  
Short Bowel Syndrome ◽  
Failure To Thrive ◽  
Favorable Outcome ◽  
Mortality And Morbidity ◽  
Short Bowel ◽  
Recurrent Vomiting ◽  
High Degree ◽  
Significant Mortality

Congenital short bowel syndrome (SBS) is a rare congen.it.al disease, Only about 37 cases were reported. Infants usually present with failure to 'thrive, recurrent vomiting and or diarrhoea. It is associated with significant mortality and morbidity, High degree of suspicion is necessary to diagnose this condition promptly. Early initiation of parenteral nutrition or surgery may result in a favorable outcome. We treated a case of infant aged eight-weeks presented with recurrent bilious vomiting and failure to thrive. On Laparotomy it was found that the baby had very short small bowel with malrotation. This case was reported and reviewed. Journal of Surgical Sciences (2014) Vol. 18 (1) : 35-37

scholarly journals Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction

2020 ◽  
Vol 48 (9) ◽  
pp. 030006052095472
Author(s):  
Mostafa Zain ◽  
Mansour Abdelkader ◽  
Ahmed Azab ◽  
Mostafa Kotb
Keyword(s):  
Short Bowel Syndrome ◽  
Failure To Thrive ◽  
Gastrointestinal Disorder ◽  
Chronic Diarrhoea ◽  
Small Bowel Length ◽  
Short Bowel ◽  
Ileocecal Junction ◽  
Intestinal Length ◽  
Neonatal Intestinal Obstruction ◽  
Ladd’S Procedure

Congenital short bowel syndrome (CSBS) is an uncommon gastrointestinal disorder in which an unclear aetiology causes considerable intrauterine reduction in small bowel length. As a result of reduced absorptive intestinal length, chronic diarrhoea, vomiting, and consequently, failure to thrive are likely. We report a case of CSBS in a 26-day-old girl who had malrotation and a short bowel with a length of bowel from the pylorus to the ileocecal junction of approximately 40 cm. The patient underwent Ladd’s procedure, but she is still dependent on parenteral nutrition.

428: HYPERAMMONEMIC ENCEPHALOPATHY AND NEW-ONSET SEIZURES IN A ROUX-EN-Y AND SHORT BOWEL SYNDROME PATIENT

2018 ◽  
Vol 46 (1) ◽  
pp. 198-198 ◽  
Author(s):  
Joseph Grogg ◽  
Jason Feinman ◽  
Ibrahim El Husseini ◽  
Sabiha Hussain
Keyword(s):  
Short Bowel Syndrome ◽  
Syndrome Patient ◽  
Short Bowel ◽  
Hyperammonemic Encephalopathy ◽  
New Onset

Short bowel syndrome after Billroth II gastric resection

2004 ◽  
Vol 42 (05) ◽  
Author(s):  
Z Nagy ◽  
A Illés ◽  
Á Király ◽  
L Nagy
Keyword(s):  
Short Bowel Syndrome ◽  
Gastric Resection ◽  
Billroth Ii ◽  
Short Bowel
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