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

L. Smith; M. A. Lambert; P. Brochu; G. Jasmin; I. A. Qureshi; E. G. Seidman

doi:10.1097/00005176-199211000-00011

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

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

Pediatrics

Research output: Contribution to journal › Article

23 Scopus citations

Original language	English (US)
Pages (from-to)	431-436
Number of pages	6
Journal	Journal of pediatric gastroenterology and nutrition
Volume	15
Issue number	4
DOIs	https://doi.org/10.1097/00005176-199211000-00011
State	Published - Nov 1992

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Gastroenterology

Access to Document

10.1097/00005176-199211000-00011

Cite this

Smith, L., Lambert, M. A., Brochu, P., Jasmin, G., Qureshi, I. A., & Seidman, E. G. (1992). Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome: Presentation as acute liver disease with coagulopathy. Journal of pediatric gastroenterology and nutrition, 15(4), 431-436. https://doi.org/10.1097/00005176-199211000-00011

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