neurofibromatosis type 1
神經纖維瘤病第一型
neurofibromatosis type 2
神經纖維瘤病第二型
diagnosed with neurofibromatosis
確診神經纖維瘤病
suffering from neurofibromatosis
罹患神經纖維瘤病
neurofibromatosis patient
神經纖維瘤病患者
neurofibromatosis symptoms
神經纖維瘤病症狀
neurofibromatosis treatment
神經纖維瘤病治療
genetic neurofibromatosis
遺傳性神經纖維瘤病
congenital neurofibromatosis
先天性神經纖維瘤病
familial neurofibromatosis
家族性神經纖維瘤病
neurofibromatosis type 1 is characterized by café-au-lait spots and skin neurofibromas.
神經纖維瘤病第一型的特徵是咖啡牛奶斑和皮膚神經纖維瘤。
the genetic disorder neurofibromatosis can cause benign tumors to grow on nerve tissue.
遺傳性疾病神經纖維瘤病可能導致良性腫瘤在神經組織上生長。
doctors recommend regular monitoring for patients with neurofibromatosis to detect complications early.
醫生建議對神經纖維瘤病患者進行定期監測，以早期發現併發症。
neurofibromatosis type 2 often presents with bilateral vestibular schwannomas.
神經纖維瘤病第二型常表現為雙側前庭神經鞘瘤。
genetic counseling is essential for families affected by neurofibromatosis.
對受神經纖維瘤病影響的家庭來說，遺傳諮詢是必不可少的。
some cases of neurofibromatosis may lead to learning disabilities in children.
某些神經纖維瘤病病例可能會導致兒童學習障礙。
the severity of neurofibromatosis varies widely among affected individuals.
神經纖維瘤病的嚴重程度在受影響個體之間差異很大。
research into neurofibromatosis has led to new targeted therapy options.
對神經纖維瘤病的研究導致了新的靶向治療選擇。
skin examinations are crucial for diagnosing and managing neurofibromatosis.
皮膚檢查對於診斷和管理神經纖維瘤病至關重要。
neurofibromatosis can affect multiple organ systems including the skin and nervous system.
神經纖維瘤病可能影響多個器官系統，包括皮膚和神經系統。
plexiform neurofibromas are a common manifestation of neurofibromatosis type 1.
軸索型神經纖維瘤是神經纖維瘤病第一型的常見表現。
ophthalmologic exams help detect lisch nodules in neurofibromatosis patients.
眼科檢查有助於在神經纖維瘤病患者中發現利希結節。
neurofibromatosis is caused by mutations in the nf1 gene located on chromosome 17.
神經纖維瘤病是由位於第17號染色體上的nf1基因突變引起的。
children diagnosed with neurofibromatosis require multidisciplinary care teams.
被診斷為神經纖維瘤病的兒童需要多學科護理團隊。
neurofibromatosis type 1
神經纖維瘤病第一型
neurofibromatosis type 2
神經纖維瘤病第二型
diagnosed with neurofibromatosis
確診神經纖維瘤病
suffering from neurofibromatosis
罹患神經纖維瘤病
neurofibromatosis patient
神經纖維瘤病患者
neurofibromatosis symptoms
神經纖維瘤病症狀
neurofibromatosis treatment
神經纖維瘤病治療
genetic neurofibromatosis
遺傳性神經纖維瘤病
congenital neurofibromatosis
先天性神經纖維瘤病
familial neurofibromatosis
家族性神經纖維瘤病
neurofibromatosis type 1 is characterized by café-au-lait spots and skin neurofibromas.
神經纖維瘤病第一型的特徵是咖啡牛奶斑和皮膚神經纖維瘤。
the genetic disorder neurofibromatosis can cause benign tumors to grow on nerve tissue.
遺傳性疾病神經纖維瘤病可能導致良性腫瘤在神經組織上生長。
doctors recommend regular monitoring for patients with neurofibromatosis to detect complications early.
醫生建議對神經纖維瘤病患者進行定期監測，以早期發現併發症。
neurofibromatosis type 2 often presents with bilateral vestibular schwannomas.
神經纖維瘤病第二型常表現為雙側前庭神經鞘瘤。
genetic counseling is essential for families affected by neurofibromatosis.
對受神經纖維瘤病影響的家庭來說，遺傳諮詢是必不可少的。
some cases of neurofibromatosis may lead to learning disabilities in children.
某些神經纖維瘤病病例可能會導致兒童學習障礙。
the severity of neurofibromatosis varies widely among affected individuals.
神經纖維瘤病的嚴重程度在受影響個體之間差異很大。
research into neurofibromatosis has led to new targeted therapy options.
對神經纖維瘤病的研究導致了新的靶向治療選擇。
skin examinations are crucial for diagnosing and managing neurofibromatosis.
皮膚檢查對於診斷和管理神經纖維瘤病至關重要。
neurofibromatosis can affect multiple organ systems including the skin and nervous system.
神經纖維瘤病可能影響多個器官系統，包括皮膚和神經系統。
plexiform neurofibromas are a common manifestation of neurofibromatosis type 1.
軸索型神經纖維瘤是神經纖維瘤病第一型的常見表現。
ophthalmologic exams help detect lisch nodules in neurofibromatosis patients.
眼科檢查有助於在神經纖維瘤病患者中發現利希結節。
neurofibromatosis is caused by mutations in the nf1 gene located on chromosome 17.
神經纖維瘤病是由位於第17號染色體上的nf1基因突變引起的。
children diagnosed with neurofibromatosis require multidisciplinary care teams.
被診斷為神經纖維瘤病的兒童需要多學科護理團隊。
探索常見搜尋詞彙