The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: A systematic review

被引:23
|
作者
Anbouba, Grace M. [1 ,2 ]
Carmany, Erin P. [2 ]
Natoli, Jaime L. [3 ]
机构
[1] Univ Wisconsin, Waisman Ctr, Madison, WI 53705 USA
[2] Wayne State Univ, Sch Med, Detroit, MI 48201 USA
[3] Kaiser Permanente Southern Calif, Pasadena, CA USA
关键词
hypodontia; hypohidrosis; hypotrichosis; X-linked hypohidrotic ectodermal dysplasia; CHROMOSOME INACTIVATION; MUTATIONAL SPECTRUM; DENTAL FINDINGS; PREVALENCE; PHENOTYPES;
D O I
10.1002/ajmg.a.61493
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The objective of this study was to review the published literature on X-linked hypohidrotic ectodermal dysplasia (XLHED) for the prevalence and characteristics of three features of XLHED: hypodontia, hypohidrosis, and hypotrichosis. A systematic search of English-language articles was conducted in May 2019 to identify publications with information on any of the three features of XLHED. We excluded studies with five or fewer participants, that did not specify X-linked inheritance or an EDA mutation, and discussed only management of features. The weighted means for total missing teeth, location of missing teeth, prevalence of reduced and absent sweating ability, and sparse or absent hair were analyzed across all studies. Additional findings for hypodontia, hypohidrosis, and hypotrichosis were summarized qualitatively. Twenty publications (18 studies) were accepted. Reported findings for males tended to be more informative than for carrier females. The weighted mean for missing teeth for affected males was 22.4 (range: 10-28) and carrier females was 3.4 (range: 0-22). The most common conserved teeth for males were the canines. The most common missing teeth for females were the maxillary lateral incisors. The weighted mean prevalence of reduced or absent sweating ability was 95.7% for males and 71.6% for females. The weighted mean prevalence for hypotrichosis was 88.1% for males and 61.6% for females. This systematic review provides insight into the prevalence, characteristics, and variability of the three classic features of XLHED. These findings provide detailed natural history information for families with XLHED as well as key characteristics that can aid in diagnosis.
引用
收藏
页码:831 / 841
页数:11
相关论文
共 50 条
  • [11] DENTAL FINDINGS IN X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    CRAWFORD, PJM
    ALDRED, MJ
    JOURNAL OF DENTAL RESEARCH, 1989, 68 (04) : 578 - 578
  • [12] 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)
  • [13] 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
  • [14] Anthropometric and cephalometric measurements in X-linked hypohidrotic ectodermal dysplasia
    Lexner, M. O.
    Bardow, A.
    Bjorn-Jorgensen, J.
    Hertz, J. M.
    Almer, L.
    Kreiborg, S.
    ORTHODONTICS & CRANIOFACIAL RESEARCH, 2007, 10 (04) : 203 - 215
  • [15] X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA - UNUSUAL PROSTHETIC PROBLEM
    NORTJE, CJ
    FARMAN, AG
    THOMAS, CJ
    WATERMEYER, GJJ
    JOURNAL OF PROSTHETIC DENTISTRY, 1978, 40 (02): : 137 - 142
  • [16] X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families
    Visinoni, AF
    de Souza, RLR
    Freire-Maia, N
    Gollop, TR
    Chautard-Freire-Maia, EA
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 122A (01): : 51 - 55
  • [17] MOLECULAR DELETION ANALYSIS IN X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    THOMAS, NS
    DAVIES, KP
    ZONANA, J
    CLARKE, A
    RASTAN, S
    BROCKDORFF, N
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 205 - 205
  • [18] Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia
    Yapijakis, Christos
    Gintoni, Iphigenia
    Chrousos, George
    GENEDIS 2020: GENETICS AND NEURODEGENERATIVE DISEASES, 2021, 1339
  • [19] MULTIPLE SEBACEOUS NEVI IN X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    ORGE, C
    BONSMANN, G
    HAMM, H
    HAUTARZT, 1991, 42 (10): : 645 - 647
  • [20] REGIONAL LOCALIZATION OF X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA (EDA)
    CLARKE, A
    SARFARAZI, M
    ZONANA, J
    THOMAS, NST
    ROBERTS, K
    HARPER, PS
    CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4): : 594 - 594