神经鞘脂病是一类神经鞘脂分解代谢障碍的遗传性疾病，酶学检测是确诊的一种主要手段。
Sphingolipidosis is a group of hereditary diseases characterised by the deficiency in enzymes responsible for catabolism of sphingolipids.
神经鞘脂病是一类神经鞘脂分解代谢障碍的遗传性疾病，酶学检测是确诊的一种主要手段。
Sphingolipidosis is a group of hereditary diseases characterised by the deficiency in enzymes responsible for catabolism of sphingolipids.
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