Whole saliva in X-linked hypohidrotic ectodermal dysplasia

被引:23
|
作者
Lexner, Michala Oron
Bardow, Allan
Hertz, Jens Michael
Almer, Lis
Nauntofte, Birgitte
Kreiborg, Sven
机构
[1] Univ Copenhagen, Sch Dent, Dept Paediat Dent & Clin Genet, DK-2200 Copenhagen N, Denmark
[2] Univ Copenhagen, Sch Dent, Dept Oral Med, DK-2200 Copenhagen N, Denmark
[3] Aarhus Univ Hosp, Dept Clin Genet, DK-8000 Aarhus, Denmark
关键词
GLAND HYPOFUNCTION; SYMPTOMS; PROTEIN;
D O I
10.1111/j.1365-263X.2006.00812.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background. X-linked hypohidrotic ectodermal dysplasia (HED) is the most common type of ectodermal dysplasia. Identification of female carriers of X-linked HED can be difficult because of varying degrees of clinical symptoms due to the X-chromosome inactivation. This is the first Study about whole saliva flow and composition in males affected by HED and female carriers all confirmed by molecular genetic analysis. Hypothesis and aim. As salivary glands derive from ectoderm, we hypothesized that whole saliva flow and composition are altered in males affected by HED and female carriers. Design. Saliva flow and composition were examined in a group of affected males and in a group Of female carriers, all confirmed by molecular genetic analysis, and compared with healthy male and female controls. Results. Affected males and female carriers had reduced whole saliva flow and saliva with high concentrations of most inorganic salivary constituents as well as total protein. However, affected males and female carriers seemed to have reduced amylase activity and concentration relative to their total protein concentration. Conclusion. Saliva flow and composition may be used as part of a comprehensive clinical examination to identify potential female carriers of HED.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 50 条
  • [1] CLINICAL ASPECTS OF X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    CLARKE, A
    PHILLIPS, DIM
    BROWN, R
    HARPER, PS
    ARCHIVES OF DISEASE IN CHILDHOOD, 1987, 62 (10) : 989 - 996
  • [2] IDENTIFYING CARRIERS FOR X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    PINHEIRO, M
    FREIREMAIA, N
    LANCET, 1977, 2 (8044): : 936 - 936
  • [3] RECOGNITION OF HETEROZYGOTES FOR X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    PASSARGE, E
    HUTTER, J
    CLINICAL GENETICS, 1983, 23 (03) : 218 - 218
  • [4] SALIVARY FLOW IN X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    ALDRED, MJ
    BAGG, J
    PEARCE, NX
    CRAWFORD, PJM
    JOURNAL OF DENTAL RESEARCH, 1989, 68 (04) : 578 - 578
  • [5] Functional analysis of saliva secretion in a mouse model of X-linked hypohidrotic ectodermal dysplasia
    Munemasa, Takashi
    Mukaibo, Taro
    Melvin, James E.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2018, 36 (03) : S312 - S312
  • [6] CONCURRENT HYPOHIDROTIC ECTODERMAL DYSPLASIA AND X-LINKED ICHTHYOSIS
    ESTERLY, NB
    PASHAYAN, HM
    WEST, CE
    AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1973, 126 (04): : 539 - 545
  • [7] Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia
    Schneider, Holm
    Faschingbauer, Florian
    Schuepbach-Mallepell, Sonia
    Koerber, Iris
    Wohlfart, Sigrun
    Dick, Angela
    Wahlbuhl, Mandy
    Kowalczyk-Quintas, Christine
    Vigolo, Michele
    Kirby, Neil
    Tannert, Corinna
    Rompel, Oliver
    Rascher, Wolfgang
    Beckmann, Matthias W.
    Schneider, Pascal
    NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (17): : 1604 - 1610
  • [8] DENTAL FINDINGS IN X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    CRAWFORD, PJM
    ALDRED, MJ
    JOURNAL OF DENTAL RESEARCH, 1989, 68 (04) : 578 - 578
  • [9] Lung and eye involvement in X-linked hypohidrotic ectodermal dysplasia
    J Dietz
    T Kaercher
    AT Schneider
    T Zimmermann
    K Huttner
    R Johnson
    H Schneider
    Head & Face Medicine, 8 (Suppl 1)
  • [10] An unusual manifestation of X-linked hypohidrotic ectodermal dysplasia with keratoderma
    Ferguson, L.
    de Brito, M.
    Mansour, S.
    Khan, I.
    BRITISH JOURNAL OF DERMATOLOGY, 2019, 181 : 82 - 82