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Growth hormone as a rescue treatment in maple syrup urine disease with lessons from pediatric burn literature, case report and brief literature review.
Kimbrell, Brooke E; Hicks, Faith; Foster, Cortney B; Kishk, Omayma A; Quinteros-Fernandez, Sara A; Nikita, Maria Eleni; Greene, Carol L.
Afiliación
  • Kimbrell BE; 1501 Kennewick Rd, Baltimore, MD 21218, United States of America.
  • Hicks F; Kennedy Kreiger Institute, 707 North Broadway, Baltimore MD 21205, United States of America.
  • Foster CB; Prisma Health Systems, Greenville, SC 29605, United States of America.
  • Kishk OA; Division of Pediatric Critical Care, Department of Pediatrics, University of Maryland Medical Center, Baltimore, MD 21201, United States of America.
  • Quinteros-Fernandez SA; Department of Pharmacy, University of Maryland Medical Center, Baltimore, MD 21218, United States of America.
  • Nikita ME; Department of Nutrition, University of Maryland Medical Center, Baltimore, MD 21201, United States of America.
  • Greene CL; Division of Pediatric Endocrinology, Department of Pediatrics, University of Maryland Medical Center, Baltimore, MD 21201, United States of America.
Mol Genet Metab Rep ; 25: 100685, 2020 Dec.
Article en En | MEDLINE | ID: mdl-33354514
ABSTRACT
Maple Syrup Urine Disease (MSUD) is a rare inherited disorder of branched chain amino acid metabolism characterized by cerebral edema and death in uncorrected metabolic crisis. It is conventionally treated with intensive nutritional therapy to prevent and correct metabolic crisis. This paper reports the use of growth hormone as a pharmacologic rescue agent in the case of an 11-year-old male with MSUD and metabolic crisis refractory to standard interventions. The initiation of short courses of growth hormone correlated with corrected mental status, resolution of metabolic acidosis, and improvement in plasma leucine levels on two occasions during an admission to the pediatric intensive care unit. This is the first known case report of the use of growth hormone in MSUD since contemporary dietary management became available. The discussion includes a literature review of the use of growth hormone in inherited diseases of amino acid metabolism and a brief discussion of protein anabolic pharmacotherapeutic agents shown to improve net protein balance in pediatric burn patients. We propose that growth hormone and other protein anabolic agents may be valuable adjuvants to standard therapy in children with inherited metabolic disease.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Systematic_reviews Idioma: En Revista: Mol Genet Metab Rep Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Systematic_reviews Idioma: En Revista: Mol Genet Metab Rep Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
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