-
translocase deficiency, also
called hyperornithinemia-hyperammonemia-
homocitrullinuria (HHH) syndrome, is a rare
autosomal recessive urea
cycle disorder...
-
Hungry Hippos, a 1978
tabletop game Hyperornithinemia-hyperammonemia-
homocitrullinuria syndrome, a
genetic disorder HHH(1,13), a run-length
limited code...
- (hyperammonemia, hyperornithinemia,
homocitrullinuria). Neuropediatrics. 1986 Feb;17(1):48-52. Kato T, Sano M,
Mizutani N.;
Homocitrullinuria and
homoargininuria in...
-
Argininemia (Deficiency of arginase) Hyperornithinemia, hyperammonemia,
homocitrullinuria (HHH)
syndrome (Deficiency of the
mitochondrial ornithine transporter)...
- hepatitis,
Citrin deficiency, and hyperornithinemia-hyperammonemia-
homocitrullinuria syndrome.
Treatment Hydration, arginine, and hemodialysis. Prognosis...
-
Inheritance in Man (OMIM): 238970 - hyperornithinemia-hyperammonemia-
homocitrullinuria syndrome Online Mendelian Inheritance in Man (OMIM): 237310 - hyperammonemia...
-
hyperammonemia in
adult siblings with hyperornithinemia, hyperammonemia, and
homocitrullinuria syndrome".
Archives of Neurology. 47 (10): 1134–1137. doi:10.1001/archneur...
-
Hyperlysinemia Hyperopia Hyperornithinemia Hyperornithinemia, hyperammonemia,
homocitrullinuria syndrome Hyperostosid corticalis deformans juvenilis Hyperostosis...
-
ornithine translocase deficiency (hyperornithinemia, hyperammonemia,
homocitrullinuria syndrome, HHH syndrome).
Ornithine concentrations can be an unreliable...
-
claim to
screen for HHH
syndrome (hyperammonemia, hyperornithinemia,
homocitrullinuria)
based on the
detection of
elevated ornithine levels in the newborn...
