| HHH Syndrome | Hyperamnonemia-Hyperornithinemia-Homocitrullinemia Syndrome |
|---|---|
| HHH | hyperornithinemia, hyperammonemia, homocitrillinuria [syndrome] |
| HOGA | hyperornithinemia with gyrate atrophy |
| hyperornithinemia |
excessive ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperammonemia-homocitrullinemia syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| hyperornithinemia-hyperammonemia-homocitrullinuria s. |
an autosomal recessive syndrome characterized by elevated plasma levels of ornithine, postprandial hyperammonemia and homocitrullinuria, and aversion to protein ingestion. It is believed to result from a defect in the transport of ornithine into mitochondria, which disturbs the cycle of ureagenesis. Called also HHH s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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