-
Ornithine translocase deficiency, also
called hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, is a rare
autosomal recessive urea cycle...
- a 1990
computer game
Hungry Hungry Hippos, a 1978
tabletop game
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a
genetic disorder HHH(1...
- urea
cycle disorders,
fulminant hepatitis,
Citrin deficiency, and
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
Treatment Hydration, arginine...
-
Hyperlipoproteinemia type V
Hyperlipoproteinemia Hyperlysinemia Hyperopia Hyperornithinemia Hyperornithinemia, hyperammonemia,
homocitrullinuria syndrome Hyperostosid...
-
argininosuccinic acid lyase)
Argininemia (Deficiency of arginase)
Hyperornithinemia, hyperammonemia,
homocitrullinuria (HHH)
syndrome (Deficiency of the...
-
dehydrogenase 1)
Online Mendelian Inheritance in Man (OMIM): 238970 -
hyperornithinemia-hyperammonemia-homocitrullinuria
syndrome Online Mendelian Inheritance...
- and
possibly also in humans. In
another metabolic disorder, in the
hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome,
first described in...
-
disorder characterized by high
levels of ornithine. Also
known as
hyperornithinemia, it may be ****ociated with
psychomotor ****ation or
epileptic episodes...
- VE (October 1990). "Episodic
hyperammonemia in
adult siblings with
hyperornithinemia, hyperammonemia, and
homocitrullinuria syndrome".
Archives of Neurology...
- available. Some
regions claim to
screen for HHH
syndrome (hyperammonemia,
hyperornithinemia, homocitrullinuria)
based on the
detection of
elevated ornithine levels...
