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A novel nutritional approach to infants and children with congenital diarrhea due to homozygous DGAT1 mutations.

Peri MillmanRamit M RimonChani ToffMartin EngvallRon ShaoulMichael WilschanskiHila ElyasharHarland S Winter
Published in: Journal of pediatric gastroenterology and nutrition (2024)
Children with DGAT1 deficiency respond to dietary restriction of lipids. Management with a novel nutritional approach provides effective treatment for infants with DGAT1 deficiency, treats diarrhea and PLE, promotes growth and development, avoids TPN dependency, and decreases the potential for essential fatty acid deficiency.
Keyphrases
  • fatty acid
  • replacement therapy
  • young adults
  • irritable bowel syndrome
  • clostridium difficile
  • risk assessment
  • combination therapy
  • smoking cessation
  • climate change