n.神经纤维瘤病

Neurofibromatosis is an inherited disorder characterized by the development of benign tumors on nerve sheaths.
神经纤维瘤病是一种遗传性疾病，特征是神经鞘上形成良性肿瘤。
A diagnosis of neurofibromatosis type 1 was confirmed through genetic testing.
通过基因检测确认了患有1型神经纤维瘤病的诊断。
She carries the gene for neurofibromatosis, which increases her risk of developing the condition.
她携带有神经纤维瘤病的基因，这使她有更高的患病风险。
The child's facial appearance was marked by the telltale signs of neurofibromatosis.
这孩子的面部特征明显显示出神经纤维瘤病的典型迹象。
Treatment for neurofibromatosis often involves monitoring and managing symptoms rather than surgery.
对神经纤维瘤病的治疗通常侧重于监控和管理症状，而非手术。
He underwent multiple surgeries to remove the numerous neurofibromas on his skin.
他接受了多次手术，以去除皮肤上的众多神经纤维瘤。
Hereditary neurofibromatosis can lead to learning disabilities in children.
遗传性神经纤维瘤病可能导致儿童的学习障碍。
Researchers continue to study the underlying mechanisms of neurofibromatosis in search of new treatments.
研究人员仍在研究神经纤维瘤病的潜在机制，以寻找新的治疗方法。
The patient's anxiety was partly due to the unpredictability of the growth of their neurofibromas.
患者的焦虑部分源于他们神经纤维瘤的生长具有不确定性。
Support groups provide a vital community for people living with neurofibromatosis to share their experiences and coping strategies.
支持团体为神经纤维瘤病患者提供了一个分享经历和应对策略的重要社区。