neurofibromatosis
英[njʊə\'rəʊfaɪbrəʊmətəʊsɪs]
美[njʊr\'roʊfaɪbroʊmətoʊsɪs]
基本释义
- n.
- 神经纤维瘤病
实用例句
Neurofibromatosis is one of autosomal - dominant neurogenetic diseases with relatively low incidence.
神经纤维瘤病是一常染色体显性遗传性疾病,临床上较为少见.
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Objective To explore the reason and treatment of short bowel syndrome after retroperitoneal multiple neurofibromatosis operation.
目的探讨腹膜后多发性神经纤维瘤术后致短肠综合征的原因和治疗.
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Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before.
神经纤维瘤病, 以前又称vonRecknn沙ausen病,属常染色体显性遗传病.
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英英释义
Noun
1. autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities