| Plural | neurofibromatoses |
neurofibromatosis type 1
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neurofibromatosis type 2
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diagnosed with neurofibromatosis
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suffering from neurofibromatosis
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neurofibromatosis patient
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neurofibromatosis symptoms
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neurofibromatosis treatment
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genetic neurofibromatosis
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congenital neurofibromatosis
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familial neurofibromatosis
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neurofibromatosis type 1 is characterized by café-au-lait spots and skin neurofibromas.
Neurofibromatose type 1 er karakteriseret ved café-au-lait-flekker og hudneurofibromer.
the genetic disorder neurofibromatosis can cause benign tumors to grow on nerve tissue.
Den genetiske lidelse neurofibromatose kan føre til, at良性 tumorer vokser på nervervæv.
doctors recommend regular monitoring for patients with neurofibromatosis to detect complications early.
Læger anbefaler regelmæssig overvågning af patienter med neurofibromatose for at opdage komplikationer tidligt.
neurofibromatosis type 2 often presents with bilateral vestibular schwannomas.
Neurofibromatose type 2 viser ofte sig med bilaterale vestibulære schwannomer.
genetic counseling is essential for families affected by neurofibromatosis.
Genetisk rådgivning er afgørende for familier, der er ramt af neurofibromatose.
some cases of neurofibromatosis may lead to learning disabilities in children.
Nogle tilfælde af neurofibromatose kan føre til læringshindringer hos børn.
the severity of neurofibromatosis varies widely among affected individuals.
Alvorligheden af neurofibromatose varierer meget mellem de ramte individer.
research into neurofibromatosis has led to new targeted therapy options.
Forskning i neurofibromatose har ført til nye målrettede terapioptioner.
skin examinations are crucial for diagnosing and managing neurofibromatosis.
Hudundersøgelser er afgørende for at diagnosticere og håndtere neurofibromatose.
neurofibromatosis can affect multiple organ systems including the skin and nervous system.
Neurofibromatose kan påvirke flere organ-systemer, herunder huden og nervesystemet.
plexiform neurofibromas are a common manifestation of neurofibromatosis type 1.
Plexiforme neurofibromer er en almindelig manifestation af neurofibromatose type 1.
ophthalmologic exams help detect lisch nodules in neurofibromatosis patients.
Øjenundersøgelser hjælper med at opdage Lisch-knuder hos patienter med neurofibromatose.
neurofibromatosis is caused by mutations in the nf1 gene located on chromosome 17.
Neurofibromatose skyldes mutationer i nf1-genen, der er placeret på kromosom 17.
children diagnosed with neurofibromatosis require multidisciplinary care teams.
Børn, der er diagnosticeret med neurofibromatose, kræver flerfaglige plejecentre.
neurofibromatosis type 1
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neurofibromatosis type 2
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diagnosed with neurofibromatosis
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suffering from neurofibromatosis
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neurofibromatosis patient
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neurofibromatosis symptoms
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neurofibromatosis treatment
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genetic neurofibromatosis
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congenital neurofibromatosis
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familial neurofibromatosis
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neurofibromatosis type 1 is characterized by café-au-lait spots and skin neurofibromas.
Neurofibromatose type 1 er karakteriseret ved café-au-lait-flekker og hudneurofibromer.
the genetic disorder neurofibromatosis can cause benign tumors to grow on nerve tissue.
Den genetiske lidelse neurofibromatose kan føre til, at良性 tumorer vokser på nervervæv.
doctors recommend regular monitoring for patients with neurofibromatosis to detect complications early.
Læger anbefaler regelmæssig overvågning af patienter med neurofibromatose for at opdage komplikationer tidligt.
neurofibromatosis type 2 often presents with bilateral vestibular schwannomas.
Neurofibromatose type 2 viser ofte sig med bilaterale vestibulære schwannomer.
genetic counseling is essential for families affected by neurofibromatosis.
Genetisk rådgivning er afgørende for familier, der er ramt af neurofibromatose.
some cases of neurofibromatosis may lead to learning disabilities in children.
Nogle tilfælde af neurofibromatose kan føre til læringshindringer hos børn.
the severity of neurofibromatosis varies widely among affected individuals.
Alvorligheden af neurofibromatose varierer meget mellem de ramte individer.
research into neurofibromatosis has led to new targeted therapy options.
Forskning i neurofibromatose har ført til nye målrettede terapioptioner.
skin examinations are crucial for diagnosing and managing neurofibromatosis.
Hudundersøgelser er afgørende for at diagnosticere og håndtere neurofibromatose.
neurofibromatosis can affect multiple organ systems including the skin and nervous system.
Neurofibromatose kan påvirke flere organ-systemer, herunder huden og nervesystemet.
plexiform neurofibromas are a common manifestation of neurofibromatosis type 1.
Plexiforme neurofibromer er en almindelig manifestation af neurofibromatose type 1.
ophthalmologic exams help detect lisch nodules in neurofibromatosis patients.
Øjenundersøgelser hjælper med at opdage Lisch-knuder hos patienter med neurofibromatose.
neurofibromatosis is caused by mutations in the nf1 gene located on chromosome 17.
Neurofibromatose skyldes mutationer i nf1-genen, der er placeret på kromosom 17.
children diagnosed with neurofibromatosis require multidisciplinary care teams.
Børn, der er diagnosticeret med neurofibromatose, kræver flerfaglige plejecentre.
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