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 32 条
  • [1] Prevalence and prevention of severe complications of hypohidrotic ectoderrnal dysplasia in infancy
    Blueschke, Gert
    Nuesken, Kai-Dietrich
    Schneider, Holm
    [J]. EARLY HUMAN DEVELOPMENT, 2010, 86 (07) : 397 - 399
  • [2] Genotype-Phenotype Correlation in Boys With X-Linked Hypohidrotic Ectodermal Dysplasia
    Burger, Kristin
    Schneider, Anne-Theres
    Wohlfart, Sigrun
    Kiesewetter, Franklin
    Huttner, Kenneth
    Johnson, Ramsey
    Schneider, Holm
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (10) : 2424 - 2432
  • [3] X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings
    Clauss, F.
    Chassaing, N.
    Smahi, A.
    Vincent, M. C.
    Calvas, P.
    Molla, M.
    Lesot, H.
    Alembik, Y.
    Hadj-Rabia, S.
    Bodemer, C.
    Maniere, M. C.
    Schmittbuhl, M.
    [J]. CLINICAL GENETICS, 2010, 78 (03) : 257 - 266
  • [4] Only Four Genes (EDA1, EDAR, EDARADD, and WNT10A) Account for 90% of Hypohidrotic/Anhidrotic Ectodermal Dysplasia Cases
    Cluzeau, Celine
    Hadj-Rabia, Smail
    Jambou, Marguerite
    Mansour, Sourour
    Guigue, Philippe
    Masmoudi, Sahben
    Bal, Elodie
    Chassaing, Nicolas
    Vincent, Marie-Claire
    Viot, Geraldine
    Clauss, Francois
    Maniere, Marie-Cecile
    Toupenay, Steve
    Le Merrer, Martine
    Lyonnet, Stanislas
    Cormier-Daire, Valerie
    Amiel, Jeanne
    Faivre, Laurence
    de Prost, Yves
    Munnich, Arnold
    Bonnefont, Jean-Paul
    Bodemer, Christine
    Smahi, Asma
    [J]. HUMAN MUTATION, 2011, 32 (01) : 70 - 77
  • [5] CLINICAL AND RADIOGRAPHIC DENTAL FINDINGS IN X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
    CRAWFORD, PJM
    ALDRED, MJ
    CLARKE, A
    [J]. JOURNAL OF MEDICAL GENETICS, 1991, 28 (03) : 181 - 185
  • [6] Deshmukh Seema, 2012, Int J Clin Pediatr Dent, V5, P197, DOI 10.5005/jp-journals-10005-1165
  • [7] Early respiratory and ocular involvement in X-linked hypohidrotic ectodermal dysplasia
    Dietz, Jasna
    Kaercher, Thomas
    Schneider, Anne-Theres
    Zimmermann, Theodor
    Huttner, Kenneth
    Johnson, Ramsey
    Schneider, Holm
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 2013, 172 (08) : 1023 - 1031
  • [8] X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED): Clinical and Diagnostic Insights from an International Patient Registry
    Fete, Mary
    Hermann, Julie
    Behrens, Jeffrey
    Huttner, Kenneth M.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (10) : 2437 - 2442
  • [9] Grange D. K., 2013, EMERY RIMOINS PRINCI
  • [10] Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia
    Guazzarotti, L.
    Tadini, G.
    Mancini, G. E.
    Giglio, S.
    Willoughby, C. E.
    Callea, M.
    Sani, I.
    Nannini, P.
    Mameli, C.
    Tenconi, A. A.
    Mauri, S.
    Bottero, A.
    Caimi, A.
    Morelli, M.
    Zuccotti, G. V.
    [J]. CLINICAL GENETICS, 2015, 87 (04) : 338 - 342