Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome: Presentation as acute liver disease with coagulopathy

Lesley J Smith, M. A. Lambert, P. Brochu, G. Jasmin, I. A. Qureshi, E. G. Seidman

Research output: Contribution to journalArticle

23 Citations (Scopus)
Original languageEnglish
Pages (from-to)431-436
Number of pages6
JournalJournal of Pediatric Gastroenterology and Nutrition
Volume15
Issue number4
StatePublished - Jan 1 1992
Externally publishedYes

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Inborn Errors Amino Acid Metabolism
Blood Coagulation Disorders
Citrulline
Ornithine
Liver Function Tests
Acute Disease
Preschool Children
Ammonia
Liver Diseases
HHH syndrome

ASJC Scopus subject areas

  • Food Science
  • Medicine (miscellaneous)
  • Gastroenterology
  • Histology
  • Pediatrics, Perinatology, and Child Health

Cite this

Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome : Presentation as acute liver disease with coagulopathy. / Smith, Lesley J; Lambert, M. A.; Brochu, P.; Jasmin, G.; Qureshi, I. A.; Seidman, E. G.

In: Journal of Pediatric Gastroenterology and Nutrition, Vol. 15, No. 4, 01.01.1992, p. 431-436.

Research output: Contribution to journalArticle

Smith, Lesley J ; Lambert, M. A. ; Brochu, P. ; Jasmin, G. ; Qureshi, I. A. ; Seidman, E. G. / Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome : Presentation as acute liver disease with coagulopathy. In: Journal of Pediatric Gastroenterology and Nutrition. 1992 ; Vol. 15, No. 4. pp. 431-436.
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