OTC基因重复是大规模超氨血病的可能原因,预后是致命的

Borkowska Natalia1, Kaluzny Lukasz2, Rokicki Dariusz3

  • 1Department of Pediatrics SPZOZ Krotoszyn, Krotoszyn, Poland.

概括

甲基因转糖酶 (OTC) 缺乏,一种常见的尿素循环障碍,可能源于未被检测到的基因重复. 识别这些罕见的遗传变异对于准确的诊断和有效的家庭查至关重要.

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