| Plural | neurofibromatoses |
neurofibromatosis type 1
neurofibromatosis tipe 1
neurofibromatosis type 2
neurofibromatosis tipe 2
diagnosed with neurofibromatosis
didagnosis menderita neurofibromatosis
suffering from neurofibromatosis
menderita neurofibromatosis
neurofibromatosis patient
pasien neurofibromatosis
neurofibromatosis symptoms
gejala neurofibromatosis
neurofibromatosis treatment
pengobatan neurofibromatosis
genetic neurofibromatosis
neurofibromatosis genetik
congenital neurofibromatosis
neurofibromatosis kongenital
familial neurofibromatosis
neurofibromatosis familial
neurofibromatosis type 1 is characterized by café-au-lait spots and skin neurofibromas.
neurofibromatosis tipe 1 menyebabkan titik-titik seperti kopi dengan susu pada kulit.
the genetic disorder neurofibromatosis can cause benign tumors to grow on nerve tissue.
dokter mendiagnosis pasien dengan neurofibromatosis setelah pemeriksaan menyeluruh.
doctors recommend regular monitoring for patients with neurofibromatosis to detect complications early.
neurofibromatosis dapat menyebabkan perkembangan tumor jinak pada jaringan saraf.
neurofibromatosis type 2 often presents with bilateral vestibular schwannomas.
konseling genetik direkomendasikan untuk keluarga yang terkena neurofibromatosis.
genetic counseling is essential for families affected by neurofibromatosis.
neurofibromatosis tipe 2 biasanya menyebabkan gangguan pendengaran karena schwannoma vestibular.
some cases of neurofibromatosis may lead to learning disabilities in children.
anak-anak dengan neurofibromatosis memerlukan pemantauan rutin oleh spesialis.
the severity of neurofibromatosis varies widely among affected individuals.
saat ini belum ada obat untuk neurofibromatosis, hanya pilihan penanganan.
research into neurofibromatosis has led to new targeted therapy options.
operasi mungkin diperlukan untuk menghilangkan tumor yang disebabkan oleh neurofibromatosis.
skin examinations are crucial for diagnosing and managing neurofibromatosis.
peneliti sedang melakukan uji klinis untuk pengobatan neurofibromatosis baru.
neurofibromatosis can affect multiple organ systems including the skin and nervous system.
neurofibromatosis mengikuti pola pewarisan autosomal dominan.
plexiform neurofibromas are a common manifestation of neurofibromatosis type 1.
nodul lisch adalah manifestasi mata umum dari neurofibromatosis tipe 1.
ophthalmologic exams help detect lisch nodules in neurofibromatosis patients.
pasien neurofibromatosis mungkin mengalami kesulitan belajar dan tantangan perilaku.
neurofibromatosis is caused by mutations in the nf1 gene located on chromosome 17.
children diagnosed with neurofibromatosis require multidisciplinary care teams.
neurofibromatosis type 1
neurofibromatosis tipe 1
neurofibromatosis type 2
neurofibromatosis tipe 2
diagnosed with neurofibromatosis
didagnosis menderita neurofibromatosis
suffering from neurofibromatosis
menderita neurofibromatosis
neurofibromatosis patient
pasien neurofibromatosis
neurofibromatosis symptoms
gejala neurofibromatosis
neurofibromatosis treatment
pengobatan neurofibromatosis
genetic neurofibromatosis
neurofibromatosis genetik
congenital neurofibromatosis
neurofibromatosis kongenital
familial neurofibromatosis
neurofibromatosis familial
neurofibromatosis type 1 is characterized by café-au-lait spots and skin neurofibromas.
neurofibromatosis tipe 1 menyebabkan titik-titik seperti kopi dengan susu pada kulit.
the genetic disorder neurofibromatosis can cause benign tumors to grow on nerve tissue.
dokter mendiagnosis pasien dengan neurofibromatosis setelah pemeriksaan menyeluruh.
doctors recommend regular monitoring for patients with neurofibromatosis to detect complications early.
neurofibromatosis dapat menyebabkan perkembangan tumor jinak pada jaringan saraf.
neurofibromatosis type 2 often presents with bilateral vestibular schwannomas.
konseling genetik direkomendasikan untuk keluarga yang terkena neurofibromatosis.
genetic counseling is essential for families affected by neurofibromatosis.
neurofibromatosis tipe 2 biasanya menyebabkan gangguan pendengaran karena schwannoma vestibular.
some cases of neurofibromatosis may lead to learning disabilities in children.
anak-anak dengan neurofibromatosis memerlukan pemantauan rutin oleh spesialis.
the severity of neurofibromatosis varies widely among affected individuals.
saat ini belum ada obat untuk neurofibromatosis, hanya pilihan penanganan.
research into neurofibromatosis has led to new targeted therapy options.
operasi mungkin diperlukan untuk menghilangkan tumor yang disebabkan oleh neurofibromatosis.
skin examinations are crucial for diagnosing and managing neurofibromatosis.
peneliti sedang melakukan uji klinis untuk pengobatan neurofibromatosis baru.
neurofibromatosis can affect multiple organ systems including the skin and nervous system.
neurofibromatosis mengikuti pola pewarisan autosomal dominan.
plexiform neurofibromas are a common manifestation of neurofibromatosis type 1.
nodul lisch adalah manifestasi mata umum dari neurofibromatosis tipe 1.
ophthalmologic exams help detect lisch nodules in neurofibromatosis patients.
pasien neurofibromatosis mungkin mengalami kesulitan belajar dan tantangan perilaku.
neurofibromatosis is caused by mutations in the nf1 gene located on chromosome 17.
children diagnosed with neurofibromatosis require multidisciplinary care teams.
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