Item request has been placed!
×
Item request cannot be made.
×
Processing Request
Case of congenital short small intestine: survival with use of long-term parenteral feeding.
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
- Author(s): Dorney SF; Byrne WJ; Ament ME
- Source:
Pediatrics [Pediatrics] 1986 Mar; Vol. 77 (3), pp. 386-9.
- Publication Type:
Case Reports; Journal Article
- Language:
English
- Additional Information
- Source:
Publisher: American Academy of Pediatrics Country of Publication: United States NLM ID: 0376422 Publication Model: Print Cited Medium: Print ISSN: 0031-4005 (Print) Linking ISSN: 00314005 NLM ISO Abbreviation: Pediatrics Subsets: MEDLINE
- Publication Information:
Publication: Elk Grove Village Il : American Academy of Pediatrics
Original Publication: Springfield, Ill., Thomas.
- Subject Terms:
- Abstract:
Isolated congenital short small intestine is a rare anomaly. Of six (one male, five females) previously reported cases, four died in infancy from intractable diarrhea. We report the case of 7-year-old boy with this syndrome in whom a 2-year period of parenteral feeding at home allowed normal weight gain, growth, and development while intestinal adaptation occurred. Parenteral feeding was discontinued at age 2 1/3 years, and for the past 5 years his weight has remained between the tenth and 25th percentiles and his stature between the 25th and 50th percentiles. His development has been normal and he functions at or above grade level at school. Coefficient of fat absorption has increased from 54% to 81%. Vitamin B12 absorption has improved but has not normalized. He remains lactose intolerant. We believe his survival, growth, and development would have been compromised if he had not received a prolonged period of parenteral feeding.
- Accession Number:
0 (Dietary Fats)
- Publication Date:
Date Created: 19860301 Date Completed: 19860404 Latest Revision: 20041117
- Publication Date:
20240829
- Accession Number:
3081870
No Comments.