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1000 Titel
  • Presenting symptoms in children with neurofibromatosis type 2
1000 Autor/in
  1. Gugel, Isabel |
  2. Grimm, Florian |
  3. Teuber, Christian |
  4. Zipfel, Julian |
  5. Tatagiba, Marcos |
  6. Mautner, Victor-Felix |
  7. Schuhmann, Martin Ulrich |
  8. Kluwe, Lan |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-06-15
1000 Erschienen in
1000 Quellenangabe
  • 36(10):2463-2470
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00381-020-04729-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575472/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!The hallmark of neurofibromatosis type 2 (NF2) is the presence of bilateral vestibular schwannomas (VS) which however have not yet developed or grown to large size in children and young adolescents. Therefore, early diagnosis in pediatric patients without family history of NF2 has to be made by signs and symptoms not related to VS which will be reviewed in this study.!##!Methods!#!A total of 70 children diagnosed for NF2 at an age of < 18 years were identified from our patient cohort. Age and symptoms, signs and pathology at symptom onset, age at NF2 diagnosis and symptoms leading to diagnosis as well as genetic findings were retrospectively reviewed.!##!Results!#!The average age at symptom/sign onset was 8 ± 6 (range 0-17) years and 11 ± 5 (range 1-17) years at time of diagnosis. Fifteen children had a positive family history and were diagnosed upon additional clinical symptoms. The most frequent first presenting symptom/signs were ophthalmological abnormalities (49%), followed by cutaneous features (40%), non-VS-related neurological deficits (33%), and symptoms attributable to VS (21%). VS were not only the most common symptomatic neoplasm but also the most frequent pathological evidence for the diagnosis (72%). In 42 patients with available genetic testing results, pathogenic mutations were most frequently identified (n = 27).!##!Conclusion!#!The presenting symptoms in NF2 children appear 'unspecific' or less specific for classical NF2 compared with adult NF2 patients, posing a challenge particularly for cases without family history. In children, ophthalmological and cutaneous features should raise clinical suspicion for NF2 and referral to an NF2 specialized center is recommended.
1000 Sacherschließung
lokal Infant, Newborn [MeSH]
lokal Adolescent [MeSH]
lokal Mutation [MeSH]
lokal Neurofibromatosis 2/diagnosis [MeSH]
lokal Neurofibromatosis type 2
lokal Vestibular schwannoma
lokal Annual Issue Paper
lokal Neurofibromatosis 2/complications [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Retrospective Studies [MeSH]
lokal Infant [MeSH]
lokal Child [MeSH]
lokal Pediatric
lokal Neurofibromatosis 2/genetics [MeSH]
lokal Presenting symptom
lokal Child, Preschool [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-2923-5949|https://frl.publisso.de/adhoc/uri/R3JpbW0sIEZsb3JpYW4=|https://frl.publisso.de/adhoc/uri/VGV1YmVyLCBDaHJpc3RpYW4=|https://frl.publisso.de/adhoc/uri/WmlwZmVsLCBKdWxpYW4=|https://frl.publisso.de/adhoc/uri/VGF0YWdpYmEsIE1hcmNvcw==|https://frl.publisso.de/adhoc/uri/TWF1dG5lciwgVmljdG9yLUZlbGl4|https://frl.publisso.de/adhoc/uri/U2NodWhtYW5uLCBNYXJ0aW4gVWxyaWNo|https://frl.publisso.de/adhoc/uri/S2x1d2UsIExhbg==
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  1. Presenting symptoms in children with neurofibromatosis type 2
1000 Objektart article
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1000 Erstellt am 2023-11-17T03:20:25.375+0100
1000 Erstellt von 322
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1000 Zuletzt bearbeitet Fri Dec 01 04:52:01 CET 2023
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