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PMID: 22052830 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Objective assessment of nasality in Flemish adults with neurofibromatosis type 1.

American journal of medical genetics. Part A ·Vol. 155A ·No. 12 ·2011-12-00 ·页码 2974-81

Cosyns M, Mortier G, Janssens S, Claes K, Van Borsel J

Abstract

When characterizing the speech of a patient with neurofibromatosis type 1 (NF1), hypernasality is often mentioned. As few studies applied technically assisted evaluations of nasality in NF1 patients, the aim of the present study was to document the nasal resonance of adults with NF1 using nasometry. The nasometric data obtained from the NF1 patients were compared with the nasalance scores of a healthy control group and with normative data. The final study group consisted of 24 adult NF1 patients and 16 controls, all living in the East Flemish part of Belgium. Nasalance scores were obtained while the participants sustained three vowels (/a:/, /i./, and /u./) and one consonant (/m/) and read three standard nasalance passages. Despite the inter- and intra-subject variability, we observed that NF1 patients as a group exhibited higher mean nasalance scores than controls. This finding was especially clear in males. Potential genotype-phenotype correlations between NF1 mutation type and hypernasality were examined but could not be demonstrated. Conversely, comparison of the nasometric data obtained from the NF1 patients with magnetic resonance imaging findings showed some degree of interesting correlation. We conclude that, notwithstanding the small sample size for some analyses, nasality is an area of interest in the NF1 population. As altered nasality influences speech intelligibility, nasality requires attention during follow-up visits, particularly when it concerns a male NF1 patient.

MeSH 主题词
Adolescent Adult Age Factors Aged Belgium Brain/abnormalities,pathology Case-Control Studies Female Genetic Association Studies Humans Male Middle Aged Mutation Neurofibromatosis 1/complications,ethnology,genetics Sex Factors Voice Disorders/complications,ethnology,genetics Young Adult
作者与单位
共 5 位作者,点击展开单位 / ORCID
Cosyns Marjan
Department of Otorhinolaryngology and Logopaedic & Audiologic Sciences, Ghent University, Ghent, Belgium. marjan.cosyns@ugent.be
Mortier Geert
Janssens Sandra
Claes Kathleen
Van Borsel John
Article Info
Journal
American journal of medical genetics. Part A
Abbr.
Am J Med Genet A
ISSN
1552-4833
Corresponding email
Published
2011-12-00
电子出版
2011-00-03
页码
2974-81
Language
English
Country/Region
United States
NLM ID
101235741
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