neurofibromatosis type 1
1型神经纤维瘤病
neurofibromatosis type 2
2型神经纤维瘤病
diagnosed with neurofibromatosis
被诊断为神经纤维瘤病
living with neurofibromatosis
与神经纤维瘤病共存
neurofibromatosis patient
神经纤维瘤病患者
neurofibromatosis research
神经纤维瘤病研究
neurofibromatosis awareness
神经纤维瘤病意识
neurofibromatosis symptoms
神经纤维瘤病症状
neurofibromatosis treatment
神经纤维瘤病治疗
hereditary neurofibromatosis
遗传性神经纤维瘤病
neurofibromatosis type 1 is an autosomal dominant genetic disorder characterized by café-au-lait spots and skin neurofibromas.
1型神经纤维瘤病是一种常染色体显性遗传疾病，其特征为咖啡牛奶斑和皮肤神经纤维瘤。
doctors often recommend genetic counseling for families affected by neurofibromatoses to understand inheritance patterns.
医生通常建议受神经纤维瘤病影响的家庭进行遗传咨询，以了解遗传模式。
regular mri monitoring is essential for patients with neurofibromatoses to detect tumor growth early.
定期核磁共振监测对于神经纤维瘤病患者至关重要，以便早期发现肿瘤生长。
neurofibromatosis type 2 typically causes bilateral vestibular schwannomas that can lead to hearing loss.
2型神经纤维瘤病通常会导致双侧前庭神经鞘瘤，从而可能引起听力损失。
research studies continue to explore new treatment options for managing neurofibromatoses and their complications.
研究继续探索治疗神经纤维瘤病及其并发症的新方案。
schwannomatosis is considered a distinct form of neurofibromatoses that primarily affects peripheral nerves.
神经鞘瘤病被认为是神经纤维瘤病的一种独特类型，主要影响周围神经。
children diagnosed with neurofibromatoses should receive regular eye examinations to check for optic pathway gliomas.
确诊神经纤维瘤病的儿童应定期进行眼部检查，以排查视通路胶质瘤。
the variability in symptoms makes neurofibromatoses challenging to diagnose and predict in some patients.
症状的多变性使神经纤维瘤病在某些患者中难以诊断和预测。
support groups provide valuable resources for individuals and families coping with neurofibromatoses.
支持小组为应对神经纤维瘤病的个人和家庭提供宝贵的资源。
neurofibromas are benign tumors that commonly develop in patients with various types of neurofibromatoses.
神经纤维瘤是良性肿瘤，常见于不同类型神经纤维瘤病患者。
lisch nodules are harmless pigmented iris hamartomas frequently associated with neurofibromatoses type 1.
lisch结节是无害的色素性虹膜错构瘤，常与1型神经纤维瘤病相关。
multidisciplinary medical teams are best suited to manage the complex manifestations of neurofibromatoses.
多学科医疗团队最适合管理神经纤维瘤病的复杂表现。
neurofibromatosis type 1
1型神经纤维瘤病
neurofibromatosis type 2
2型神经纤维瘤病
diagnosed with neurofibromatosis
被诊断为神经纤维瘤病
living with neurofibromatosis
与神经纤维瘤病共存
neurofibromatosis patient
神经纤维瘤病患者
neurofibromatosis research
神经纤维瘤病研究
neurofibromatosis awareness
神经纤维瘤病意识
neurofibromatosis symptoms
神经纤维瘤病症状
neurofibromatosis treatment
神经纤维瘤病治疗
hereditary neurofibromatosis
遗传性神经纤维瘤病
neurofibromatosis type 1 is an autosomal dominant genetic disorder characterized by café-au-lait spots and skin neurofibromas.
1型神经纤维瘤病是一种常染色体显性遗传疾病，其特征为咖啡牛奶斑和皮肤神经纤维瘤。
doctors often recommend genetic counseling for families affected by neurofibromatoses to understand inheritance patterns.
医生通常建议受神经纤维瘤病影响的家庭进行遗传咨询，以了解遗传模式。
regular mri monitoring is essential for patients with neurofibromatoses to detect tumor growth early.
定期核磁共振监测对于神经纤维瘤病患者至关重要，以便早期发现肿瘤生长。
neurofibromatosis type 2 typically causes bilateral vestibular schwannomas that can lead to hearing loss.
2型神经纤维瘤病通常会导致双侧前庭神经鞘瘤，从而可能引起听力损失。
research studies continue to explore new treatment options for managing neurofibromatoses and their complications.
研究继续探索治疗神经纤维瘤病及其并发症的新方案。
schwannomatosis is considered a distinct form of neurofibromatoses that primarily affects peripheral nerves.
神经鞘瘤病被认为是神经纤维瘤病的一种独特类型，主要影响周围神经。
children diagnosed with neurofibromatoses should receive regular eye examinations to check for optic pathway gliomas.
确诊神经纤维瘤病的儿童应定期进行眼部检查，以排查视通路胶质瘤。
the variability in symptoms makes neurofibromatoses challenging to diagnose and predict in some patients.
症状的多变性使神经纤维瘤病在某些患者中难以诊断和预测。
support groups provide valuable resources for individuals and families coping with neurofibromatoses.
支持小组为应对神经纤维瘤病的个人和家庭提供宝贵的资源。
neurofibromas are benign tumors that commonly develop in patients with various types of neurofibromatoses.
神经纤维瘤是良性肿瘤，常见于不同类型神经纤维瘤病患者。
lisch nodules are harmless pigmented iris hamartomas frequently associated with neurofibromatoses type 1.
lisch结节是无害的色素性虹膜错构瘤，常与1型神经纤维瘤病相关。
multidisciplinary medical teams are best suited to manage the complex manifestations of neurofibromatoses.
多学科医疗团队最适合管理神经纤维瘤病的复杂表现。
探索常用高频词汇