Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency
Yudai Koya, Michihiko Shibata, Michio Senju, Yuichi Honma, Masaaki Hiura, Masahiro Ishii, Shirou Matsumoto, Masaru Harada
Abstract
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Yudai Koya, Michihiko Shibata, Michio Senju, Yuichi Honma, Masaaki Hiura, Masahiro Ishii, Shirou Matsumoto, Masaru Harada
Abstract
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A 52-year-old woman developed vomiting and disturbance of consciousness after consuming raw fish and sushi on a trip. A blood test showed hyperammonemia (310 μg/dL) with a normal liver function. She fell into a deep coma, and her serum ammonia level increased to 684 μg/dL. L-arginine was administered as a diagnostic treatment for urea cycle disorder (UCD) and serum ammonia, and her consciousness levels improved. She was diagnosed with ornithine transcarbamylase deficiency (OTCD) by analyses of plasma amino acids, urinary orotic acid, and the OTC gene mutation. UCD should be considered for patients with hyperammonemia without severe liver function abnormalities.
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A 52-year-old woman developed vomiting and disturbance of consciousness after consuming raw fish and sushi on a trip. A blood test showed hyperammonemia (310 μg/dL) with a normal liver function. She fell into a deep coma, and her serum ammonia level increased to 684 μg/dL. L-arginine was administered as a diagnostic treatment for urea cycle disorder (UCD) and serum ammonia, and her consciousness levels improved. She was diagnosed with ornithine transcarbamylase deficiency (OTCD) by analyses of plasma amino acids, urinary orotic acid, and the OTC gene mutation. UCD should be considered for patients with hyperammonemia without severe liver function abnormalities.
Key concepts: Ornithine transcarbamylase deficiency, Hyperammonemia, Urea cycle, Medicine, Ornithine transcarbamylase, Orotic acid, Internal medicine, Citrullinemia