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ornithine carbamoyltransferase deficiency disease/homa

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NakalaMajaribio ya klinikiHati miliki
2 matokeo

Histopathological findings in a male with late-onset ornithine transcarbamylase deficiency.

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Late onset of symptoms in a 12 1/2-year-old male with ornithine transcarbamylase (OTC) deficiency were associated with unusual histological features in the liver. The patient presented with an acute onset of hyperammonemia and altered mental status after a 2-day prodrome of vomiting and lethargy.
OBJECTIVE Liver transplantation could be a useful treatment for selected inborn errors of metabolism. This study evaluated the outcome and viral infections after liver transplantation in young children and infants with these diseases. METHODS The outcome of liver transplantation and clinical
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