[Ornithine transcarbamylase deficiency].

Megan McCrillis, John D. Thompson
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Abstract

Ornithine transcarbamylase deficiency can become evident at any age. The most severe form occurs in the first few days of life. This neonatal-onset form of the disorder usually affects males; it is very rare in females. An infant with the neonatal-onset form of ornithine transcarbamylase deficiency may be lacking in energy (lethargic) or unwilling to eat, and have a poorly-controlled breathing rate or body temperature. Infants with this disorder may be described as "floppy" and can experience seizures or coma. Complications from ornithine transcarbamylase deficiency may include developmental delay and intellectual disability. Progressive liver damage may also occur.
鸟氨酸转氨基甲酰基酶缺乏症。
鸟氨酸转氨基甲酰基酶缺乏症可以在任何年龄变得明显。最严重的形式发生在生命的最初几天。这种新生儿发病形式的疾病通常影响男性;这在女性中非常罕见。新生儿型鸟氨酸转氨基甲酰基酶缺乏症的婴儿可能缺乏能量(嗜睡)或不愿进食,呼吸频率或体温控制不佳。患有这种疾病的婴儿可能被描述为“软瘫”,并可能出现癫痫发作或昏迷。鸟氨酸转氨基甲酰基酶缺乏的并发症可能包括发育迟缓和智力残疾。进行性肝损害也可能发生。
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