Literature DB >> 2051453

Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.

P J Crawford1, M J Aldred, A Clarke.   

Abstract

X linked hypohidrotic ectodermal dysplasia was studied in the dentition of both affected males and carrier females. Hypodontia was more severe in males than females and there were differences in the pattern of tooth absence between the sexes. Abnormal crown form, with the maximum diameter of the teeth being apically displaced, was noted particularly in the anterior teeth. Taurodontism was commonly seen radiographically.

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Year:  1991        PMID： 2051453      PMCID： PMC1016802          DOI： 10.1136/jmg.28.3.181

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  10 in total

1.  Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism.

Authors:  P J Crawford; R D Evans; M J Aldred
Journal:  Br Dent J       Date:  1988-02-06       Impact factor: 1.626

2.  Hypodontia, ectodermal dysplasia and sweat pore count.

Authors:  M S Tso; P J Crawford; J Miller
Journal:  Br Dent J       Date:  1985-01-19       Impact factor: 1.626

3.  Dental anomalies of number, form and size: their prevalence in British schoolchildren.

Authors:  A H Brook
Journal:  J Int Assoc Dent Child       Date:  1974-12

4.  Taurodontism and concomitant hypodontia in siblings.

Authors:  A Stenvik; B U Zachrisson; B Svatun
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1972-05

5.  Taurodontism.

Authors:  R D Tennant
Journal:  Dent Dig       Date:  1966-08

6.  Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia.

Authors:  J A Sofaer
Journal:  Br Dent J       Date:  1981-11-17       Impact factor: 1.626

7.  A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.

Authors:  M Nakata; H Koshiba; K Eto; W E Nance
Journal:  Am J Hum Genet       Date:  1980-11       Impact factor: 11.025

8.  Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers.

Authors:  A L Söderholm; I Kaitila
Journal:  Clin Genet       Date:  1985-08       Impact factor: 4.438

9.  Oligodontia: a study of its prevalence and variation in 4032 children.

Authors:  N E Silverman; J L Ackerman
Journal:  ASDC J Dent Child       Date:  1979 Nov-Dec

Review 10.  Taurodontism, an isolated trait associated with syndromes and X-chromosomal aneuploidy.

Authors:  M T Jaspers; C J Witkop
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025
  10 in total
  14 in total

1.  Overlap syndrome: a diagnostic dilemma.

Authors:  Kaushal Mahendra Shah; Sampada Kanitkar
Journal:  BMJ Case Rep       Date:  2012-11-27

2.  Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.

Authors:  J Zonana; M Jones; A Clarke; J Gault; B Muller; N S Thomas
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

3.  The Impact of the Eda Pathway on Tooth Root Development.

Authors:  J M Fons Romero; H Star; R Lav; S Watkins; M Harrison; M Hovorakova; D Headon; A S Tucker
Journal:  J Dent Res       Date:  2017-08-16       Impact factor: 6.116

4.  Familial ectodermal dysplasia: a peers' agony.

Authors:  Karthik Hegde; Roopashri Rajesh Kashyap; Gopakumar Nair; Preeti P Nair
Journal:  BMJ Case Rep       Date:  2013-07-23

5.  Upper cervical spine and craniofacial morphology in hypohidrotic ectodermal dysplasia.

Authors:  L Sonnesen; A Jasemi; H Gjørup; J Daugaard-Jensen
Journal:  Eur Arch Paediatr Dent       Date:  2018-08-20

6.  Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.

Authors:  B M Ferguson; N S Thomas; F Munoz; D Morgan; A Clarke; J Zonana
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

7.  High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Authors:  J Zonana; M Jones; D Browne; M Litt; P Kramer; H W Becker; N Brockdorff; S Rastan; K P Davies; A Clarke
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

8.  Case series: Treatment considerations in x-linked hypohidrotic ectodermal dysplasia.

Authors:  M O Lexner; L Almer
Journal:  Eur Arch Paediatr Dent       Date:  2009-11

9.  Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.

Authors:  J Zonana; J Gault; K J Davies; M Jones; D Browne; M Litt; N Brockdorff; S Rastan; A Clarke; N S Thomas
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

10.  Karyotyping, dermatoglyphic, and sweat pore analysis of five families affected with ectodermal dysplasia.

Authors:  Manpreet Sidhu; Alka D Kale; Vijayalakshmi S Kotrashetti
Journal:  J Oral Maxillofac Pathol       Date:  2012-09
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