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| Research article summary (published 28 Mar 1991): |
[The classification of atypical forms of neurofibromatosis]
(Zur Klassierung atypischer Neurofibromatose-Formen.)
Full Abstract
Neurofibromatosis (NF) represents not an entity but a group of several forms which differ as to symptoms, prognosis and inheritance. In 1982 Riccardi suggested a classification into eight categories. Two of these--Von Recklinghausen NF-1 and bilateral acoustic NF-2- were defined in 1987 by a National Institutes of Health Consensus Development Conference. We describe 13 patients whose symptoms do not fit the diagnostic criteria for NF-1 and NF-2. 6 subjects can be classified as segmental NF-V. One of these patients was remarkable in having iris hamartomata, while his daughter was affected with NF-1. Another (female) patient in this group had areolar freckling, a finding not yet reported in NF patients. 4 cases belong to the late-onset NF-VII category, 3 of whom developed a neurofibrosarcoma. Two subjects are fist-degree relatives (mother and son). We are not aware of familial occurrence of NF-VII. Two further subjects were assigned to the variant form of NF, NF-IV. One patient had symptoms similar to NF-2 but the minimal diagnostic criteria were not fulfilled. Nevertheless, we consider his classification as NF-2 in view of a pattern of intracranial calcification repeatedly and exclusively found in NF-2. In general, assignment to a category of NF is important for appropriate patient management and genetic counselling. Classification of individual patients may be arbitrary at the time.
Author information
Author/s: Theiler, R (R); Stocker, H (H); Boltshauser, E (E);
Affiliation: Universitätskinderklinik Zürich.
Journal and publication information
Publication Type: Case Reports; English Abstract; Journal Article; Research Support, Non-U.S. Gov't
Journal: Schweizerische medizinische Wochenschrift (Schweiz Med Wochenschr), published in SWITZERLAND. (Language: ger)
Reference: 1991-Mar; vol 121 (issue 13) : pp 446-55
Dates: Created 1991/06/20; Completed 1991/06/20; Revised 2006/11/15;
PMID: 1903213, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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