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
確診為神經纖維瘤病
living with neurofibromatosis
與神經纖維瘤病共存
neurofibromatosis patient
神經纖維瘤病患者
neurofibromatosis research
神經纖維瘤病研究
neurofibromatosis awareness
神經纖維瘤病意識
neurofibromatosis symptoms
神經纖維瘤病症狀
neurofibromatosis treatment
神經纖維瘤病治療
hereditary neurofibromatosis
遺傳性神經纖維瘤病
neurofibromatosis type 1 is an autosomal dominant genetic disorder characterized by café-au-lait spots and skin neurofibromas.
神經纖維瘤病第一型是一種常染色體顯性遺傳疾病，特徵為咖啡牛奶斑和皮膚神經纖維瘤。
doctors often recommend genetic counseling for families affected by neurofibromatoses to understand inheritance patterns.
醫生通常會建議受神經纖維瘤病影響的家庭接受遺傳諮詢，以了解遺傳模式。
regular mri monitoring is essential for patients with neurofibromatoses to detect tumor growth early.
對於神經纖維瘤病患者來說，定期進行MRI監測對於早期發現腫瘤生長至關重要。
neurofibromatosis type 2 typically causes bilateral vestibular schwannomas that can lead to hearing loss.
神經纖維瘤病第二型通常會導致雙側前庭神經瘤，可能導致聽力喪失。
research studies continue to explore new treatment options for managing neurofibromatoses and their complications.
研究持續探索管理神經纖維瘤病及其併發症的新治療方法。
schwannomatosis is considered a distinct form of neurofibromatoses that primarily affects peripheral nerves.
神經鞘瘤病被視為一種獨特的神經纖維瘤病形式，主要影響周圍神經。
children diagnosed with neurofibromatoses should receive regular eye examinations to check for optic pathway gliomas.
診斷出神經纖維瘤病的兒童應定期接受眼科檢查，以檢查視神經通路膠質瘤。
the variability in symptoms makes neurofibromatoses challenging to diagnose and predict in some patients.
症狀的多樣性使神經纖維瘤病在某些患者中診斷和預測變得具有挑戰性。
support groups provide valuable resources for individuals and families coping with neurofibromatoses.
支持小組為應對神經纖維瘤病的個人和家庭提供寶貴的資源。
neurofibromas are benign tumors that commonly develop in patients with various types of neurofibromatoses.
神經纖維瘤是良性腫瘤，常見於各種類型的神經纖維瘤病患者。
lisch nodules are harmless pigmented iris hamartomas frequently associated with neurofibromatoses type 1.
利希結節是無害的色素性虹膜錯構瘤，常見於神經纖維瘤病第一型。
multidisciplinary medical teams are best suited to manage the complex manifestations of neurofibromatoses.
多學科醫療團隊最適合管理神經纖維瘤病的複雜表現。
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
確診為神經纖維瘤病
living with neurofibromatosis
與神經纖維瘤病共存
neurofibromatosis patient
神經纖維瘤病患者
neurofibromatosis research
神經纖維瘤病研究
neurofibromatosis awareness
神經纖維瘤病意識
neurofibromatosis symptoms
神經纖維瘤病症狀
neurofibromatosis treatment
神經纖維瘤病治療
hereditary neurofibromatosis
遺傳性神經纖維瘤病
neurofibromatosis type 1 is an autosomal dominant genetic disorder characterized by café-au-lait spots and skin neurofibromas.
神經纖維瘤病第一型是一種常染色體顯性遺傳疾病，特徵為咖啡牛奶斑和皮膚神經纖維瘤。
doctors often recommend genetic counseling for families affected by neurofibromatoses to understand inheritance patterns.
醫生通常會建議受神經纖維瘤病影響的家庭接受遺傳諮詢，以了解遺傳模式。
regular mri monitoring is essential for patients with neurofibromatoses to detect tumor growth early.
對於神經纖維瘤病患者來說，定期進行MRI監測對於早期發現腫瘤生長至關重要。
neurofibromatosis type 2 typically causes bilateral vestibular schwannomas that can lead to hearing loss.
神經纖維瘤病第二型通常會導致雙側前庭神經瘤，可能導致聽力喪失。
research studies continue to explore new treatment options for managing neurofibromatoses and their complications.
研究持續探索管理神經纖維瘤病及其併發症的新治療方法。
schwannomatosis is considered a distinct form of neurofibromatoses that primarily affects peripheral nerves.
神經鞘瘤病被視為一種獨特的神經纖維瘤病形式，主要影響周圍神經。
children diagnosed with neurofibromatoses should receive regular eye examinations to check for optic pathway gliomas.
診斷出神經纖維瘤病的兒童應定期接受眼科檢查，以檢查視神經通路膠質瘤。
the variability in symptoms makes neurofibromatoses challenging to diagnose and predict in some patients.
症狀的多樣性使神經纖維瘤病在某些患者中診斷和預測變得具有挑戰性。
support groups provide valuable resources for individuals and families coping with neurofibromatoses.
支持小組為應對神經纖維瘤病的個人和家庭提供寶貴的資源。
neurofibromas are benign tumors that commonly develop in patients with various types of neurofibromatoses.
神經纖維瘤是良性腫瘤，常見於各種類型的神經纖維瘤病患者。
lisch nodules are harmless pigmented iris hamartomas frequently associated with neurofibromatoses type 1.
利希結節是無害的色素性虹膜錯構瘤，常見於神經纖維瘤病第一型。
multidisciplinary medical teams are best suited to manage the complex manifestations of neurofibromatoses.
多學科醫療團隊最適合管理神經纖維瘤病的複雜表現。
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